NP-MRD: Showing NP-Card for 7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol (NP0285628)

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Record Information

Version

2.0

Created at

2022-09-09 13:53:04 UTC

Updated at

2022-09-09 13:53:04 UTC

NP-MRD ID

NP0285628

Secondary Accession Numbers

None

Natural Product Identification

Common Name

7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol

Description

7-Bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-octahydro-1H-inden-4-ol belongs to the class of organic compounds known as sesquiterpenoids. These are terpenes with three consecutive isoprene units. 7-Bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-octahydro-1H-inden-4-ol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 55 57  0  0  0  0  0  0  0  0999 V2000
    4.4646    1.2738   -0.4986 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4825    0.4035    0.2938 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0421    1.2783    1.4674 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3379    0.0943   -0.6212 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.5781   -1.1263   -0.2719 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2836   -1.3082   -0.4324 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6743   -0.3247   -0.9910 C   0  0  1  0  0  0  0  0  0  0  0  0
   -1.4396   -0.8594   -2.1680 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8728   -0.5047   -1.9080 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9985   -0.6297   -0.4032 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0229   -2.1135   -0.0905 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2346   -0.0232    0.1387 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.8129   -0.9255    1.7468 Br  0  0  0  0  0  0  0  0  0  0  0  0
   -4.1555    1.4472    0.4189 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9150    1.8071    1.1660 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7302    1.4262    0.3156 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.4770    1.7791    1.0801 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7044    2.0944   -0.8939 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7123   -0.0609    0.0883 C   0  0  2  0  0  0  0  0  0  0  0  0
    2.3522   -2.2833    0.3220 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8468   -2.0470    0.1036 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1837   -0.7913    0.8499 C   0  0  1  0  0  0  0  0  0  0  0  0
    6.0907   -0.4876    0.8909 Br  0  0  0  0  0  0  0  0  0  0  0  0
    4.9008    2.0667    0.1295 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9252    1.7746   -1.3404 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2487    0.6479   -0.9579 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.9513    1.6571    1.9827 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5179    0.6197    2.1726 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4608    2.1512    1.1408 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7028    0.9961   -0.6479 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7185   -0.0539   -1.6768 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1271   -2.2806   -0.1236 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1339    0.5606   -1.3065 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2867   -1.9495   -2.3051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1319   -0.3471   -3.1010 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1665    0.4821   -2.2801 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5147   -1.2589   -2.4372 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8231   -2.3213    0.9799 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4011   -2.7111   -0.7784 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0796   -2.4739   -0.2608 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0516   -0.1582   -0.6270 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.0279    1.7027    1.0758 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2818    2.0674   -0.4944 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9080    2.8481    1.4792 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8661    1.1595    2.0802 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1669    2.4657    0.4575 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1428    0.8789    1.3143 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7396    2.3521    1.9647 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2070    2.9356   -0.9053 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4506   -0.5436    1.0518 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2161   -2.3177    1.4243 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0031   -3.2011   -0.1505 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.1083   -2.0321   -0.9580 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3829   -2.8852    0.5913 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.8388   -0.9505    1.9031 H   0  0  0  0  0  0  0  0  0  0  0  0
 10 11  1  6
 10  9  1  0
  9  8  1  0
  8  7  1  0
  7  6  1  0
  6  5  2  0
  5 20  1  0
 20 21  1  0
 21 22  1  0
 22 23  1  0
 22  2  1  0
  2  1  1  0
  2  3  1  0
  2  4  1  0
  7 19  1  0
 19 16  1  0
 16 17  1  0
 16 18  1  6
 16 15  1  0
 15 14  1  0
 14 12  1  0
 12 13  1  0
 19 10  1  0
 12 10  1  0
  4  5  1  0
 11 38  1  0
 11 39  1  0
 11 40  1  0
  9 36  1  0
  9 37  1  0
  8 34  1  0
  8 35  1  0
  7 33  1  6
  6 32  1  0
 20 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  1
  1 24  1  0
  1 25  1  0
  1 26  1  0
  3 27  1  0
  3 28  1  0
  3 29  1  0
  4 30  1  0
  4 31  1  0
 19 50  1  1
 17 46  1  0
 17 47  1  0
 17 48  1  0
 18 49  1  0
 15 44  1  0
 15 45  1  0
 14 42  1  0
 14 43  1  0
 12 41  1  6
M  END


  Mrv1533004241500172D          

 23 25  0  0  0  0            999 V2000
   -1.3110   -1.0555    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2822   -1.8800    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.0992   -1.7651    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4752   -1.7084    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0768   -2.3215    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8838   -2.1500    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -1.3654    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6538   -0.6979    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.1387   -0.0305    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.8371    0.5350    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.1271    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378    0.9521    0.0000 Br  0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -0.2854    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3523   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.6378   -1.5229    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.1681   -2.1549    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1075   -2.1549    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9233   -1.1104    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1781   -3.1062    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9851   -3.2777    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5371   -2.6646    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3441   -2.8361    0.0000 Br  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
  6  7  1  4  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
 12 14  1  0  0  0  0
 14 15  1  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
 16 19  1  0  0  0  0
  7 19  1  0  0  0  0
 10 19  1  0  0  0  0
  5 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  1  0  0  0  0
  2 22  1  0  0  0  0
 22 23  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0285628

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC12CCC(C=C3CCC(Br)C(C)(C)C3)C1C(C)(O)CCC2Br

> <INCHI_IDENTIFIER>
InChI=1S/C20H32Br2O/c1-18(2)12-13(5-6-15(18)21)11-14-7-9-19(3)16(22)8-10-20(4,23)17(14)19/h11,14-17,23H,5-10,12H2,1-4H3

> <INCHI_KEY>
IPTFWOYTNXBMID-UHFFFAOYSA-N

> <FORMULA>
C20H32Br2O

> <MOLECULAR_WEIGHT>
448.283

> <EXACT_MASS>
446.081992

> <JCHEM_ACCEPTOR_COUNT>
1

> <JCHEM_ATOM_COUNT>
55

> <JCHEM_AVERAGE_POLARIZABILITY>
43.04409238506851

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-octahydro-1H-inden-4-ol

> <ALOGPS_LOGP>
5.80

> <JCHEM_LOGP>
5.627346389666666

> <ALOGPS_LOGS>
-6.46

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
3

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_ACIDIC>
14.750990567738683

> <JCHEM_PKA_STRONGEST_BASIC>
-2.9077167256711

> <JCHEM_POLAR_SURFACE_AREA>
20.23

> <JCHEM_REFRACTIVITY>
105.48149999999998

> <JCHEM_ROTATABLE_BOND_COUNT>
1

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
1.56e-04 g/l

> <JCHEM_TRADITIONAL_IUPAC>
7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1H-inden-4-ol

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 24-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   24-APR-15         0                                  
HETATM    1  C   UNK     0      -2.447  -1.970   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.393  -3.509   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -3.918  -3.295   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -0.887  -3.189   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.143  -4.334   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.650  -4.013   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       2.126  -2.549   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.220  -1.303   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.126  -0.057   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       3.590  -0.533   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       3.429   0.999   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.924   0.237   0.000  0.00  0.00           C+0
HETATM   13 Br   UNK     0       4.924   1.777   0.000  0.00  0.00          Br+0
HETATM   14  C   UNK     0       6.258  -0.533   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       6.258  -2.073   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       4.924  -2.843   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.914  -4.023   0.000  0.00  0.00           C+0
HETATM   18  O   UNK     0       3.934  -4.023   0.000  0.00  0.00           O+0
HETATM   19  C   UNK     0       3.590  -2.073   0.000  0.00  0.00           C+0
HETATM   20  C   UNK     0      -0.333  -5.798   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -1.839  -6.118   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -2.869  -4.974   0.000  0.00  0.00           C+0
HETATM   23 Br   UNK     0      -4.376  -5.294   0.000  0.00  0.00          Br+0
CONECT    1    2                                                            
CONECT    2    1    3    4   22                                             
CONECT    3    2                                                            
CONECT    4    2    5                                                       
CONECT    5    4    6   20                                                  
CONECT    6    5    7                                                       
CONECT    7    6    8   19                                                  
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12   19                                             
CONECT   11   10                                                            
CONECT   12   10   13   14                                                  
CONECT   13   12                                                            
CONECT   14   12   15                                                       
CONECT   15   14   16                                                       
CONECT   16   15   17   18   19                                             
CONECT   17   16                                                            
CONECT   18   16                                                            
CONECT   19   16    7   10                                                  
CONECT   20    5   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21    2   23                                                  
CONECT   23   22                                                            
MASTER        0    0    0    0    0    0    0    0   23    0   50    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₀H₃₂Br₂O

Average Mass

448.2830 Da

Monoisotopic Mass

446.08199 Da

IUPAC Name

7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-octahydro-1H-inden-4-ol

Traditional Name

7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1H-inden-4-ol

CAS Registry Number

Not Available

SMILES

CC12CCC(C=C3CCC(Br)C(C)(C)C3)C1C(C)(O)CCC2Br

InChI Identifier

InChI=1S/C20H32Br2O/c1-18(2)12-13(5-6-15(18)21)11-14-7-9-19(3)16(22)8-10-20(4,23)17(14)19/h11,14-17,23H,5-10,12H2,1-4H3

InChI Key

IPTFWOYTNXBMID-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 sesquiterpenoids. These are terpenes with three consecutive isoprene units.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Prenol lipids

Sub Class

Sesquiterpenoids

Direct Parent

Sesquiterpenoids

Alternative Parents

Substituents

Sesquiterpenoid
Tertiary alcohol
Cyclic alcohol
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
Organobromide
Organohalogen compound
Alkyl halide
Alkyl bromide
Alcohol
Aliphatic homopolycyclic compound

Molecular Framework

Aliphatic homopolycyclic 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	5.8	ALOGPS
logP	5.63	ChemAxon
logS	-6.5	ALOGPS
pKa (Strongest Acidic)	14.75	ChemAxon
pKa (Strongest Basic)	-2.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	20.23 Å²	ChemAxon
Rotatable Bond Count	1	ChemAxon
Refractivity	105.48 m³·mol⁻¹	ChemAxon
Polarizability	43.04 Å³	ChemAxon
Number of Rings	3	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	ChemAxon
Veber's Rule	Yes	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 7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol (NP0285628)

MOL for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

3D MOL for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

3D SDF for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

3D-SDF for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

PDB for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

3D PDB for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

SMILES for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

INCHI for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

Structure for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)

3D Structure for NP0285628 (7-bromo-3-[(4-bromo-3,3-dimethylcyclohexylidene)methyl]-4,7a-dimethyl-hexahydro-1h-inden-4-ol)