NP-MRD: Showing NP-Card for 2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate (NP0311240)

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Record Information

Version

2.0

Created at

2022-09-11 07:06:08 UTC

Updated at

2022-09-11 07:06:08 UTC

NP-MRD ID

NP0311240

Secondary Accession Numbers

None

Natural Product Identification

Common Name

2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate

Description

2-{1-Hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]Hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate belongs to the class of organic compounds known as cycloheptafurans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom. 2-{1-Hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]Hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161513582D          

 30 33  0  0  0  0            999 V2000
    4.9037    5.3476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    4.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    4.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7058    3.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974    2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9120    3.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7099    2.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9162    2.2732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7141    1.4734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4064    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1994    1.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6608    0.4915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4853    0.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1529   -0.1586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3776    0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6962   -0.4406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5997   -1.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -1.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1604   -1.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674   -1.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472   -1.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628   -0.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3636    0.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0221    1.1754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8441    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7045    2.1513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9255    0.6605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9426   -0.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2933    3.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  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
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 20 21  1  0  0  0  0
 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
  9 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 28 29  1  0  0  0  0
 16 29  1  0  0  0  0
 23 29  1  0  0  0  0
  2 30  1  0  0  0  0
M  END

     RDKit          3D

 64 67  0  0  0  0  0  0  0  0999 V2000
    7.1203   -2.5021   -1.7684 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9233   -1.6450   -1.5942 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.0040   -0.2288   -2.0341 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8318   -2.1472   -1.0625 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5985   -1.3541   -0.8575 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5992   -1.8870   -0.3456 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.5373   -0.0843   -1.2096 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7902    0.9831   -1.2621 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6114    1.2913   -0.9350 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.4691    0.6368   -0.3344 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.3080    0.9968    1.1129 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2010    1.7340    1.8616 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6945    1.8418    3.1325 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2754    2.5384    4.3188 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4551    1.1934    3.1381 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7236    0.6778    1.9651 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8888   -0.1032    1.5680 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.3886   -1.2725    0.9739 O   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8790   -0.5269    2.5544 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7032   -1.4275    1.8608 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2612   -1.0063    0.7129 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5669   -0.2841    1.0775 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6993   -2.2574   -0.0608 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4669   -0.1538   -0.2299 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.6925   -0.8771   -1.2693 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4119   -0.3366   -1.7114 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8412    0.9004   -1.1103 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4601    1.8892   -2.2087 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7642    1.6463   -0.2163 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6396    0.7703    0.5772 C   0  0  2  0  0  0  0  0  0  0  0  0
    7.5989   -2.2812   -2.7383 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8438   -3.5889   -1.7973 H   0  0  0  0  0  0  0  0  0  0  0  0
    7.8567   -2.3502   -0.9379 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.7966    0.4587   -1.1637 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.9993    0.0087   -2.4699 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2430   -0.0056   -2.8055 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8232   -3.2021   -0.7545 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3694    1.8597   -1.7294 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.3543    2.3920   -1.1556 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5715   -0.4484   -0.3566 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.1292    2.1593    1.5437 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8981    3.4112    3.9872 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.8252    1.8621    4.9871 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4676    3.0046    4.9523 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2782   -1.9938    1.6233 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4750    0.3032    2.9834 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4325   -1.1336    3.3880 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4310    0.7904    1.1733 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.3626   -0.5455    0.3306 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.9352   -0.6732    2.0477 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8453   -2.0617   -1.1214 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9758   -3.0790    0.1549 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6640   -2.5920    0.3705 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2231    0.5082   -0.7561 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5688   -1.9440   -0.9039 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4030   -1.0387   -2.1436 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4604   -0.1729   -2.8316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6046   -1.1306   -1.6448 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2946    1.8705   -2.9801 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4414    1.5945   -2.7555 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4667    2.9289   -1.8235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4248    2.2941   -0.8626 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1839    2.3630    0.3941 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3104    1.4265    1.2027 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  2  4  2  3
  4  5  1  0
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  5  7  1  0
  7  8  1  0
  8  9  2  0
  9 10  1  0
 10 11  1  0
 11 16  2  0
 16 15  1  0
 15 13  1  0
 13 14  1  0
 13 12  2  0
 16 17  1  0
 17 18  1  6
 17 19  1  0
 19 20  1  0
 20 21  1  0
 21 22  1  0
 21 23  1  0
 21 24  1  0
 24 25  1  0
 25 26  1  0
 26 27  1  0
 27 28  1  6
 27 29  1  0
 29 30  1  0
 27 10  1  0
 12 11  1  0
 30 17  1  0
 30 24  1  0
  1 31  1  0
  1 32  1  0
  1 33  1  0
  3 34  1  0
  3 35  1  0
  3 36  1  0
  4 37  1  0
  8 38  1  0
  9 39  1  0
 10 40  1  1
 14 42  1  0
 14 43  1  0
 14 44  1  0
 12 41  1  0
 18 45  1  0
 19 46  1  0
 19 47  1  0
 22 48  1  0
 22 49  1  0
 22 50  1  0
 23 51  1  0
 23 52  1  0
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 24 54  1  6
 25 55  1  0
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 26 58  1  0
 28 59  1  0
 28 60  1  0
 28 61  1  0
 29 62  1  0
 29 63  1  0
 30 64  1  1
M  END


  Mrv1533004161513582D          

 30 33  0  0  0  0            999 V2000
    4.9037    5.3476    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7016    4.5477    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.9079    4.3228    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7058    3.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.2974    2.9480    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.9120    3.2980    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7099    2.4982    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9162    2.2732    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7141    1.4734    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4064    0.9480    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1994    1.1755    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6608    0.4915    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4853    0.4628    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1529   -0.1586    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.3776    0.1235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.6962   -0.4406    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.4218   -0.8333    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.5997   -1.2923    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8514   -1.6722    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1604   -1.1877    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1674   -1.9448    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6472   -1.0192    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1628   -0.3317    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3636    0.3687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0221    1.1754    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8441    1.3382    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7045    2.1513    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9255    0.6605    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9426   -0.1150    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2933    3.9728    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  2  0  0  0  0
  3  4  1  0  0  0  0
  4  5  2  0  0  0  0
  4  6  1  0  0  0  0
  7  6  1  4  0  0  0
  7  8  2  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
 11 12  2  0  0  0  0
 12 13  1  0  0  0  0
 12 14  1  0  0  0  0
 14 15  1  0  0  0  0
 10 15  2  0  0  0  0
 15 16  1  0  0  0  0
 16 17  1  0  0  0  0
 16 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
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 20 22  1  0  0  0  0
 20 23  1  0  0  0  0
 23 24  1  0  0  0  0
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  9 26  1  0  0  0  0
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 16 29  1  0  0  0  0
 23 29  1  0  0  0  0
  2 30  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0311240

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CC(=O)OC=CC1C2=C(OC(C)=C2)C2(O)COC(C)(C)C3CCC1(C)CC23

> <INCHI_IDENTIFIER>
InChI=1S/C25H34O5/c1-15(2)11-21(26)28-10-8-18-17-12-16(3)30-22(17)25(27)14-29-23(4,5)19-7-9-24(18,6)13-20(19)25/h8,10-12,18-20,27H,7,9,13-14H2,1-6H3

> <INCHI_KEY>
HHCQPXDZMHHIQI-UHFFFAOYSA-N

> <FORMULA>
C25H34O5

> <MOLECULAR_WEIGHT>
414.542

> <EXACT_MASS>
414.240624195

> <JCHEM_ACCEPTOR_COUNT>
3

> <JCHEM_ATOM_COUNT>
64

> <JCHEM_AVERAGE_POLARIZABILITY>
46.74090921556732

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate

> <ALOGPS_LOGP>
4.45

> <JCHEM_LOGP>
4.220399775333334

> <ALOGPS_LOGS>
-4.65

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
12.205426190425918

> <JCHEM_PKA_STRONGEST_BASIC>
-2.8596962293422803

> <JCHEM_POLAR_SURFACE_AREA>
68.9

> <JCHEM_REFRACTIVITY>
116.54660000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
4

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
9.28e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 16-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   16-APR-15         0                                  
HETATM    1  C   UNK     0       9.154   9.982   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       8.776   8.489   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       7.295   8.069   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       6.917   6.576   0.000  0.00  0.00           C+0
HETATM    5  O   UNK     0       8.022   5.503   0.000  0.00  0.00           O+0
HETATM    6  O   UNK     0       5.436   6.156   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       5.059   4.663   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       3.577   4.243   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       3.200   2.750   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       4.492   1.770   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       5.972   2.194   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       6.833   0.918   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       8.373   0.864   0.000  0.00  0.00           C+0
HETATM   14  O   UNK     0       5.885  -0.296   0.000  0.00  0.00           O+0
HETATM   15  C   UNK     0       4.438   0.231   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       3.166  -0.822   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       4.521  -1.555   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       2.986  -2.412   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0       1.589  -3.121   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0       0.299  -2.217   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -0.312  -3.630   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.208  -1.902   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0       0.304  -0.619   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -0.679   0.688   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      -0.041   2.194   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0       1.576   2.498   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0       1.315   4.016   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0       1.728   1.233   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0       1.760  -0.215   0.000  0.00  0.00           C+0
HETATM   30  C   UNK     0       9.881   7.416   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   30                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5    6                                                  
CONECT    5    4                                                            
CONECT    6    4    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10   26                                                  
CONECT   10    9   11   15                                                  
CONECT   11   10   12                                                       
CONECT   12   11   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   10   16                                                  
CONECT   16   15   17   18   29                                             
CONECT   17   16                                                            
CONECT   18   16   19                                                       
CONECT   19   18   20                                                       
CONECT   20   19   21   22   23                                             
CONECT   21   20                                                            
CONECT   22   20                                                            
CONECT   23   20   24   29                                                  
CONECT   24   23   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25    9   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   29                                                       
CONECT   29   28   16   23                                                  
CONECT   30    2                                                            
MASTER        0    0    0    0    0    0    0    0   30    0   66    0
END

View in JSmol

Synonyms

Value	Source
2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0,.0,]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoic acid	Generator
2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoic acid	Generator

Chemical Formula

C₂₅H₃₄O₅

Average Mass

414.5420 Da

Monoisotopic Mass

414.24062 Da

IUPAC Name

2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate

Traditional Name

2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate

CAS Registry Number

Not Available

SMILES

CC(C)=CC(=O)OC=CC1C2=C(OC(C)=C2)C2(O)COC(C)(C)C3CCC1(C)CC23

InChI Identifier

InChI=1S/C25H34O5/c1-15(2)11-21(26)28-10-8-18-17-12-16(3)30-22(17)25(27)14-29-23(4,5)19-7-9-24(18,6)13-20(19)25/h8,10-12,18-20,27H,7,9,13-14H2,1-6H3

InChI Key

HHCQPXDZMHHIQI-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 cycloheptafurans. These are organic heterocyclic compounds containing a cycloheptane derivative fused to a furan. Furan is a five-membered aromatic ring with four carbon atoms and one oxygen atom.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Cycloheptafurans

Sub Class

Not Available

Direct Parent

Cycloheptafurans

Alternative Parents

Substituents

Cycloheptafuran
Fatty acid ester
Oxane
Fatty acyl
Enol ester
Furan
Tertiary alcohol
Enoate ester
Alpha,beta-unsaturated carboxylic ester
Heteroaromatic compound
Carboxylic acid ester
Monocarboxylic acid or derivatives
Ether
Dialkyl ether
Carboxylic acid derivative
Oxacycle
Organooxygen compound
Organic oxide
Alcohol
Hydrocarbon derivative
Carbonyl group
Organic oxygen 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	4.45	ALOGPS
logP	4.22	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	12.21	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	3	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	68.9 Å²	ChemAxon
Rotatable Bond Count	4	ChemAxon
Refractivity	116.55 m³·mol⁻¹	ChemAxon
Polarizability	46.74 Å³	ChemAxon
Number of Rings	4	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	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

73077990

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate (NP0311240)

MOL for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

3D MOL for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

3D SDF for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

3D-SDF for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

PDB for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

3D PDB for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

SMILES for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

INCHI for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

Structure for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)

3D Structure for NP0311240 (2-{1-hydroxy-4,8,12,12-tetramethyl-3,13-dioxatetracyclo[6.6.2.0²,⁶.0¹¹,¹⁵]hexadeca-2(6),4-dien-7-yl}ethenyl 3-methylbut-2-enoate)