NP-MRD: Showing NP-Card for 5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione (NP0161990)

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Record Information

Version

2.0

Created at

2022-09-02 20:18:21 UTC

Updated at

2022-09-02 20:18:21 UTC

NP-MRD ID

NP0161990

Secondary Accession Numbers

None

Natural Product Identification

Common Name

5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione

Description

5B,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione belongs to the class of organic compounds known as naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings. 5B,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004161504482D          

 29 32  0  0  0  0            999 V2000
   -0.0339   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7762   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3163   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1265   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5569   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -2.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -0.0454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    0.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071    1.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274    0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6204    0.6235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4221   -0.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6877   -1.1368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2573   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4472   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
M  END

     RDKit          3D

 61 64  0  0  0  0  0  0  0  0999 V2000
    5.4671    7.1438   -2.5136 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.6720    5.6829   -2.5391 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.7815    4.8083   -2.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.0286    3.4138   -2.1143 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4304    2.3466   -1.7687 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1863    2.0283   -1.1465 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2836    2.9666   -0.7335 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0952    2.5672   -0.1363 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2390    3.3941    0.2570 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.8742    1.2186    0.0162 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8113    0.3059   -0.4157 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8860    0.7356   -0.9571 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4809   -1.0314   -0.2124 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.1619   -1.4820   -0.5303 C   0  0  1  0  0  0  0  0  0  0  0  0
    0.1722   -1.6470   -2.0672 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0242   -2.8750   -0.0278 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6242   -3.0458    1.2991 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7897   -2.1774    1.5601 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.9923   -2.9877    1.8987 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7311   -3.6500    3.2615 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3140   -4.0999    0.9483 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1466   -2.0769    2.1228 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2962   -2.5217    2.2406 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9132   -0.6442    2.2042 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8819   -0.0546    1.3099 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0870   -1.1208    0.5385 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0287   -1.5637   -0.5708 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8859   -0.5087   -0.1104 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3554    0.6836    0.6609 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4408    7.3932   -2.2228 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.1494    7.6271   -1.7636 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6300    7.5497   -3.5325 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5751    5.2918   -2.9547 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9055    5.2510   -1.6667 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0577    3.1946   -2.6035 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0418    1.4029   -2.0183 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4290    4.0265   -0.8377 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1141   -2.1788   -2.3538 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1822   -0.6158   -2.4984 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6691   -2.2608   -2.4152 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4803   -3.5566   -0.7828 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0560   -3.3353    0.0363 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1924   -2.9389    2.0768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8846   -4.1426    1.3974 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5502   -1.6095    2.5169 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6935   -3.7211    3.8206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0138   -3.0496    3.8298 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3933   -4.7119    3.1070 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5554   -5.0624    1.4876 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2742   -3.8853    0.3923 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5226   -4.3666    0.2388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8881   -0.1023    2.0235 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7087   -0.4230    3.2955 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3181    0.6535    0.5770 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2007    0.5425    1.9531 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0682   -1.6095   -0.2869 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6863   -2.4275   -1.1354 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9732   -0.7056   -1.3141 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2683   -0.0219   -1.0636 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0806    0.4421    1.6900 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0927    1.5415    0.5985 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  2  0
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 12  6  1  0
 28 14  1  0
 29 10  1  0
 26 18  1  0
  1 30  1  0
  1 31  1  0
  1 32  1  0
  2 33  1  0
  3 34  1  0
  4 35  1  0
  5 36  1  0
  7 37  1  0
 15 38  1  0
 15 39  1  0
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 20 46  1  0
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 25 54  1  0
 25 55  1  0
 27 56  1  0
 27 57  1  0
 27 58  1  0
 28 59  1  6
 29 60  1  0
 29 61  1  0
M  END


  Mrv1533004161504482D          

 29 32  0  0  0  0            999 V2000
   -0.0339   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7762   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3163   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1265   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6666   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4767   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7467   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5569   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -2.3841    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.0970   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8269   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.0168   -0.0454    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.3670    0.4223    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    6.1771    0.2664    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071    1.0459    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172    0.8900    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274    0.7341    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.7974   -0.0454    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6075   -0.2014    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.6204    0.6235    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.4221   -0.0708    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8776   -0.9809    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.6877   -1.1368    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    8.3375   -1.6046    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.5274   -1.4486    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.2573   -0.6691    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7172   -1.2927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.4472   -0.5132    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9071   -1.1368    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  2  1  1  4  0  0  0
  2  3  2  0  0  0  0
  4  3  1  4  0  0  0
  4  5  2  0  0  0  0
  5  6  1  0  0  0  0
  6  7  2  0  0  0  0
  7  8  1  0  0  0  0
  8  9  2  0  0  0  0
  8 10  1  0  0  0  0
 10 11  2  0  0  0  0
 11 12  1  0  0  0  0
  6 12  1  0  0  0  0
 11 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 14 16  1  0  0  0  0
 16 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  1  0  0  0  0
 19 21  1  0  0  0  0
 19 22  1  0  0  0  0
 22 23  2  0  0  0  0
 22 24  1  0  0  0  0
 24 25  1  0  0  0  0
 25 26  1  0  0  0  0
 18 26  1  0  0  0  0
 26 27  1  0  0  0  0
 26 28  1  0  0  0  0
 14 28  1  0  0  0  0
 28 29  1  0  0  0  0
 10 29  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0161990

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC=CC=CC1=CC(=O)C2=C(O1)OC1(C)CCC3C(C)(C)C(=O)CCC3(C)C1C2

> <INCHI_IDENTIFIER>
InChI=1S/C25H32O4/c1-6-7-8-9-16-14-18(26)17-15-20-24(4)12-11-21(27)23(2,3)19(24)10-13-25(20,5)29-22(17)28-16/h6-9,14,19-20H,10-13,15H2,1-5H3

> <INCHI_KEY>
GVOVBHJIAABCIL-UHFFFAOYSA-N

> <FORMULA>
C25H32O4

> <MOLECULAR_WEIGHT>
396.527

> <EXACT_MASS>
396.23005951

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
61

> <JCHEM_AVERAGE_POLARIZABILITY>
46.012508105187194

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione

> <ALOGPS_LOGP>
5.81

> <JCHEM_LOGP>
5.4817093036666655

> <ALOGPS_LOGS>
-5.08

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
4

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.950173878196846

> <JCHEM_POLAR_SURFACE_AREA>
52.6

> <JCHEM_REFRACTIVITY>
126.95739999999996

> <JCHEM_ROTATABLE_BOND_COUNT>
2

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.33e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5H-1,12-dioxatetraphene-4,8-dione

> <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      -0.063  -2.704   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       1.449  -2.995   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       2.457  -1.831   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.969  -2.122   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       4.978  -0.958   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.490  -1.249   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       6.994  -2.704   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       8.506  -2.995   0.000  0.00  0.00           C+0
HETATM    9  O   UNK     0       9.010  -4.450   0.000  0.00  0.00           O+0
HETATM   10  C   UNK     0       9.514  -1.831   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       9.010  -0.376   0.000  0.00  0.00           C+0
HETATM   12  O   UNK     0       7.498  -0.085   0.000  0.00  0.00           O+0
HETATM   13  O   UNK     0      10.018   0.788   0.000  0.00  0.00           O+0
HETATM   14  C   UNK     0      11.531   0.497   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0      11.027   1.952   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0      12.539   1.661   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0      14.051   1.370   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0      14.555  -0.085   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0      16.067  -0.376   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      16.091   1.164   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      17.588  -0.132   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      16.571  -1.831   0.000  0.00  0.00           C+0
HETATM   23  O   UNK     0      18.084  -2.122   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0      15.563  -2.995   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0      14.051  -2.704   0.000  0.00  0.00           C+0
HETATM   26  C   UNK     0      13.547  -1.249   0.000  0.00  0.00           C+0
HETATM   27  C   UNK     0      12.539  -2.413   0.000  0.00  0.00           C+0
HETATM   28  C   UNK     0      12.035  -0.958   0.000  0.00  0.00           C+0
HETATM   29  C   UNK     0      11.027  -2.122   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3                                                       
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7   12                                                  
CONECT    7    6    8                                                       
CONECT    8    7    9   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   29                                                  
CONECT   11   10   12   13                                                  
CONECT   12   11    6                                                       
CONECT   13   11   14                                                       
CONECT   14   13   15   16   28                                             
CONECT   15   14                                                            
CONECT   16   14   17                                                       
CONECT   17   16   18                                                       
CONECT   18   17   19   26                                                  
CONECT   19   18   20   21   22                                             
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   19   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22   25                                                       
CONECT   25   24   26                                                       
CONECT   26   25   18   27   28                                             
CONECT   27   26                                                            
CONECT   28   26   14   29                                                  
CONECT   29   28   10                                                       
MASTER        0    0    0    0    0    0    0    0   29    0   64    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₅H₃₂O₄

Average Mass

396.5270 Da

Monoisotopic Mass

396.23006 Da

IUPAC Name

5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-4,5,5a,5b,6,7,8,9,9a,10,11,11a-dodecahydro-1,12-dioxatetraphene-4,8-dione

Traditional Name

5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5H-1,12-dioxatetraphene-4,8-dione

CAS Registry Number

Not Available

SMILES

CC=CC=CC1=CC(=O)C2=C(O1)OC1(C)CCC3C(C)(C)C(=O)CCC3(C)C1C2

InChI Identifier

InChI=1S/C25H32O4/c1-6-7-8-9-16-14-18(26)17-15-20-24(4)12-11-21(27)23(2,3)19(24)10-13-25(20,5)29-22(17)28-16/h6-9,14,19-20H,10-13,15H2,1-5H3

InChI Key

GVOVBHJIAABCIL-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 naphthopyrans. Naphthopyrans are compounds containing a pyran ring fused to a naphthalene moiety. Furan is a 6 membered-ring non-aromatic ring with five carbon and one oxygen atoms. Naphthalene is a polycyclic aromatic hydrocarbon made up of two fused benzene rings.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Naphthopyrans

Sub Class

Not Available

Direct Parent

Naphthopyrans

Alternative Parents

Substituents

Naphthopyran
Naphthalene
Alkyl aryl ether
Pyranone
Pyran
Heteroaromatic compound
Vinylogous ester
Ketone
Cyclic ketone
Ether
Oxacycle
Organooxygen compound
Hydrocarbon derivative
Organic oxide
Organic oxygen compound
Carbonyl group
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	5.81	ALOGPS
logP	5.48	ChemAxon
logS	-5.1	ALOGPS
pKa (Strongest Basic)	-5	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	52.6 Å²	ChemAxon
Rotatable Bond Count	2	ChemAxon
Refractivity	126.96 m³·mol⁻¹	ChemAxon
Polarizability	46.01 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

75954669

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione (NP0161990)

MOL for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

3D MOL for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

3D SDF for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

3D-SDF for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

PDB for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

3D PDB for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

SMILES for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

INCHI for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

Structure for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)

3D Structure for NP0161990 (5b,9,9,11a-tetramethyl-2-(penta-1,3-dien-1-yl)-5a,6,7,9a,10,11-hexahydro-5h-1,12-dioxatetraphene-4,8-dione)