NP-MRD: Showing NP-Card for 13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate (NP0205778)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-09-05 01:46:27 UTC

Updated at

2022-09-05 01:46:28 UTC

NP-MRD ID

NP0205778

Secondary Accession Numbers

None

Natural Product Identification

Common Name

13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate

Description

13-(Furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]Pentadecan-8-yl 3-methylbutanoate belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety. 13-(Furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]Pentadecan-8-yl 3-methylbutanoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004261513492D          

 32 35  0  0  0  0            999 V2000
    6.3260   -0.9028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643   -0.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0068    0.4900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9431   -0.4868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2069    0.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6936    0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2319    0.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669    0.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9362    0.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6290   -0.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4279   -0.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8402    0.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6722    0.3491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9794    1.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267    1.4045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6100    1.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    2.0810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307    0.7538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1788    1.4026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6533    1.6468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4700    1.7636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7618    2.4019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5785    2.5187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4477    3.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8347    3.4089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0741    1.7539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8273    2.4011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7874    1.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3972    0.7258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1141    1.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9474    1.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1274    2.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 28 32  1  0  0  0  0
M  END

     RDKit          3D

 66 69  0  0  0  0  0  0  0  0999 V2000
   -6.5212   -3.2183   -0.3175 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6507   -2.2651    0.5094 C   0  0  0  0  0  0  0  0  0  0  0  0
   -6.4798   -1.0122    0.7022 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4374   -1.9555   -0.3436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5040   -1.0350    0.3429 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7161   -0.5772    1.4966 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3508   -0.6542   -0.2949 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3756    0.2342    0.2781 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.0824   -0.4689    0.5353 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9657   -0.3374   -0.5102 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1552   -1.7283   -1.1385 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3056    0.1564    0.0515 C   0  0  1  0  0  0  0  0  0  0  0  0
    3.3053   -1.0088    0.0215 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6061   -0.4808    0.6408 C   0  0  1  0  0  0  0  0  0  0  0  0
    5.5996   -1.5710    0.7204 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3395   -2.9168    0.6652 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.5592   -3.5611    0.7772 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5106   -2.6391    0.8945 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.9582   -1.4354    0.8630 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.1226    0.4901   -0.2522 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.2521    0.9985   -1.2055 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5975    1.2118   -2.4155 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.8587    1.2910   -0.7358 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.0689    1.9293   -1.6900 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.4683    2.5918   -0.5095 C   0  0  1  0  0  0  0  0  0  0  0  0
    1.3320    2.9193    0.4025 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1740    3.4016   -0.4006 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1497    2.7650   -0.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3301    2.8349    1.4357 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2120    3.7160   -0.6388 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2971    1.4051   -0.6111 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3552    1.2450   -1.8068 O   0  0  0  0  0  0  0  0  0  0  0  0
   -6.2734   -4.2325    0.0056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3273   -3.0857   -1.4039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.5938   -2.9912   -0.1697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.3957   -2.6876    1.4820 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.2185   -0.9089   -0.1292 H   0  0  0  0  0  0  0  0  0  0  0  0
   -7.0531   -1.1711    1.6542 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.8839   -0.0968    0.7571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8175   -1.4942   -1.2883 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8986   -2.8868   -0.5931 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8045    0.4887    1.2926 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3498   -1.5485    0.7432 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3779   -0.1378    1.5129 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7316    0.3257   -1.3451 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1339   -1.9739   -1.5556 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3629   -2.4927   -0.3906 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8252   -1.7010   -2.0005 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2142    0.4124    1.1329 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5626   -1.2955   -1.0140 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.9822   -1.8373    0.6610 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3984   -0.0283    1.6280 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3574   -3.3397    0.5555 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6555   -4.6355    0.7644 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.5568   -0.5291    0.9437 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1329    3.4567   -0.7497 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.6625    3.7783    1.0592 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0966    2.1128    1.1238 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3443    3.2038   -1.4977 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0433    4.5011   -0.3277 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4153    2.7992    1.6693 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7416    2.0780    1.9720 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9800    3.8577    1.7453 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5664    4.4337    0.1007 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7937    4.2242   -1.5500 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0424    3.0765   -1.0148 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  1  0
  4  5  1  0
  5  6  2  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 10 12  1  0
 12 13  1  0
 13 14  1  0
 14 20  1  0
 20 21  1  0
 21 22  2  0
 21 23  1  0
 23 24  1  6
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  0
 28 29  1  0
 28 30  1  0
 28 31  1  0
 31 32  2  0
 14 15  1  0
 15 19  2  0
 19 18  1  0
 18 17  1  0
 17 16  2  0
 31  8  1  0
 16 15  1  0
 23 12  1  0
 25 23  1  0
  1 33  1  0
  1 34  1  0
  1 35  1  0
  2 36  1  0
  3 37  1  0
  3 38  1  0
  3 39  1  0
  4 40  1  0
  4 41  1  0
  8 42  1  1
  9 43  1  0
  9 44  1  0
 10 45  1  6
 11 46  1  0
 11 47  1  0
 11 48  1  0
 12 49  1  1
 13 50  1  0
 13 51  1  0
 14 52  1  1
 25 56  1  6
 26 57  1  0
 26 58  1  0
 27 59  1  0
 27 60  1  0
 29 61  1  0
 29 62  1  0
 29 63  1  0
 30 64  1  0
 30 65  1  0
 30 66  1  0
 19 55  1  0
 17 54  1  0
 16 53  1  0
M  END


  Mrv1533004261513492D          

 32 35  0  0  0  0            999 V2000
    6.3260   -0.9028    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7643   -0.2986    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0068    0.4900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9431   -0.4868    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2069    0.0009    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6936    0.6670    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.2319    0.1059    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7669    0.9883    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9362    0.7557    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6290   -0.0100    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4279   -0.8786    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8402    0.1049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6722    0.3491    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9794    1.1147    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4267    1.4045    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6100    1.2878    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0508    2.0810    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3307    0.7538    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1788    1.4026    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.6533    1.6468    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4700    1.7636    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7618    2.4019    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5785    2.5187    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4477    3.4157    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8347    3.4089    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0741    1.7539    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8273    2.4011    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7874    1.2815    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3972    0.7258    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1141    1.1341    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.9474    1.9421    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1274    2.0332    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  2  4  1  0  0  0  0
  4  5  1  0  0  0  0
  5  6  2  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  8  9  1  0  0  0  0
  9 10  1  0  0  0  0
 10 11  1  0  0  0  0
 10 12  1  0  0  0  0
 12 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 16 17  2  0  0  0  0
 16 18  1  0  0  0  0
 12 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
 22 23  1  0  0  0  0
 23 24  1  0  0  0  0
 23 25  1  0  0  0  0
 23 26  1  0  0  0  0
  8 26  1  0  0  0  0
 26 27  2  0  0  0  0
 14 28  1  0  0  0  0
 28 29  2  0  0  0  0
 29 30  1  0  0  0  0
 30 31  1  0  0  0  0
 31 32  2  0  0  0  0
 28 32  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0205778

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)CC(=O)OC1CC(C)C2CC(OC(=O)C22OC2CCC(C)(C)C1=O)C1=COC=C1

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O7/c1-14(2)10-21(26)30-19-11-15(3)17-12-18(16-7-9-29-13-16)31-23(28)25(17)20(32-25)6-8-24(4,5)22(19)27/h7,9,13-15,17-20H,6,8,10-12H2,1-5H3

> <INCHI_KEY>
ZMBCGUSHOFUDQY-UHFFFAOYSA-N

> <FORMULA>
C25H34O7

> <MOLECULAR_WEIGHT>
446.54

> <EXACT_MASS>
446.230453435

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
66

> <JCHEM_AVERAGE_POLARIZABILITY>
47.68681094596427

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]pentadecan-8-yl 3-methylbutanoate

> <ALOGPS_LOGP>
3.63

> <JCHEM_LOGP>
5.022703301999998

> <ALOGPS_LOGS>
-4.15

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
17.650508382326436

> <JCHEM_PKA_STRONGEST_BASIC>
-2.872197159037747

> <JCHEM_POLAR_SURFACE_AREA>
95.33999999999999

> <JCHEM_REFRACTIVITY>
114.64629999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
5

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.16e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]pentadecan-8-yl 3-methylbutanoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 26-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   26-APR-15         0                                  
HETATM    1  C   UNK     0      11.809  -1.685   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      10.760  -0.557   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      11.213   0.915   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       9.227  -0.909   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       7.853   0.002   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       8.761   1.245   0.000  0.00  0.00           O+0
HETATM    7  O   UNK     0       6.033   0.198   0.000  0.00  0.00           O+0
HETATM    8  C   UNK     0       5.165   1.845   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.614   1.411   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.041  -0.019   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       2.665  -1.640   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       1.568   0.196   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.121   0.652   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       3.695   2.081   0.000  0.00  0.00           C+0
HETATM   15  O   UNK     0       2.663   2.622   0.000  0.00  0.00           O+0
HETATM   16  C   UNK     0       1.139   2.404   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       0.095   3.885   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.617   1.407   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.334   2.618   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       1.219   3.074   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0       2.744   3.292   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0       3.289   4.484   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       4.813   4.702   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0       4.569   6.376   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       5.291   6.363   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       5.738   3.274   0.000  0.00  0.00           C+0
HETATM   27  O   UNK     0       7.144   4.482   0.000  0.00  0.00           O+0
HETATM   28  C   UNK     0       5.203   2.392   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       6.341   1.355   0.000  0.00  0.00           C+0
HETATM   30  O   UNK     0       7.680   2.117   0.000  0.00  0.00           O+0
HETATM   31  C   UNK     0       7.368   3.625   0.000  0.00  0.00           C+0
HETATM   32  C   UNK     0       5.838   3.795   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3    4                                                  
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   26                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12   10   13   18                                                  
CONECT   13   12   14                                                       
CONECT   14   13   15   28                                                  
CONECT   15   14   16                                                       
CONECT   16   15   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   12   19   20                                             
CONECT   19   18   20                                                       
CONECT   20   19   18   21                                                  
CONECT   21   20   22                                                       
CONECT   22   21   23                                                       
CONECT   23   22   24   25   26                                             
CONECT   24   23                                                            
CONECT   25   23                                                            
CONECT   26   23    8   27                                                  
CONECT   27   26                                                            
CONECT   28   14   29   32                                                  
CONECT   29   28   30                                                       
CONECT   30   29   31                                                       
CONECT   31   30   32                                                       
CONECT   32   31   28                                                       
MASTER        0    0    0    0    0    0    0    0   32    0   70    0
END

View in JSmol

Synonyms

Value	Source
13-(Furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0,]pentadecan-8-yl 3-methylbutanoic acid	Generator
13-(Furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]pentadecan-8-yl 3-methylbutanoic acid	Generator

Chemical Formula

C₂₅H₃₄O₇

Average Mass

446.5400 Da

Monoisotopic Mass

446.23045 Da

IUPAC Name

13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]pentadecan-8-yl 3-methylbutanoate

Traditional Name

13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0¹,³]pentadecan-8-yl 3-methylbutanoate

CAS Registry Number

Not Available

SMILES

CC(C)CC(=O)OC1CC(C)C2CC(OC(=O)C22OC2CCC(C)(C)C1=O)C1=COC=C1

InChI Identifier

InChI=1S/C25H34O7/c1-14(2)10-21(26)30-19-11-15(3)17-12-18(16-7-9-29-13-16)31-23(28)25(17)20(32-25)6-8-24(4,5)22(19)27/h7,9,13-15,17-20H,6,8,10-12H2,1-5H3

InChI Key

ZMBCGUSHOFUDQY-UHFFFAOYSA-N

Experimental Spectra

Not Available

Predicted Spectra

Spectrum Type	Description	Depositor ID	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 25 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, H₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Chemical Shift Submissions

Not Available

Species

Species of Origin

Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as delta valerolactones. These are cyclic organic compounds containing an oxan-2- one moiety.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Lactones

Sub Class

Delta valerolactones

Direct Parent

Delta valerolactones

Alternative Parents

Substituents

Delta valerolactone
Fatty acid ester
Alpha-acyloxy ketone
Delta_valerolactone
Dicarboxylic acid or derivatives
Fatty acyl
Oxane
Heteroaromatic compound
Furan
Carboxylic acid ester
Ketone
Cyclic ketone
Oxacycle
Ether
Oxirane
Dialkyl ether
Carboxylic acid derivative
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
Organooxygen compound
Aromatic heteropolycyclic compound

Molecular Framework

Aromatic heteropolycyclic compounds

External Descriptors

Not Available

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	3.63	ALOGPS
logP	5.02	ChemAxon
logS	-4.2	ALOGPS
pKa (Strongest Acidic)	17.65	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	95.34 Å²	ChemAxon
Rotatable Bond Count	5	ChemAxon
Refractivity	114.65 m³·mol⁻¹	ChemAxon
Polarizability	47.69 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

HMDB ID

Not Available

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

Not Available

KNApSAcK ID

Not Available

Chemspider ID

Not Available

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

Not Available

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate (NP0205778)

MOL for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

3D MOL for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

3D SDF for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

3D-SDF for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

PDB for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

3D PDB for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

SMILES for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

INCHI for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

Structure for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)

3D Structure for NP0205778 (13-(furan-3-yl)-6,6,10-trimethyl-7,15-dioxo-2,14-dioxatricyclo[9.4.0.0?,?]pentadecan-8-yl 3-methylbutanoate)