NP-MRD: Showing NP-Card for 1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol (NP0181849)

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Record Information

Version

2.0

Created at

2022-09-03 20:26:40 UTC

Updated at

2022-09-03 20:26:40 UTC

NP-MRD ID

NP0181849

Secondary Accession Numbers

None

Natural Product Identification

Common Name

1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol

Description

1,3,5-Tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring. 1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol is found in Evodiella muelleri. 1,3,5-Tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI


  Mrv1533004231522272D          

 27 27  0  0  0  0            999 V2000
    2.3054    3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2414    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5236   -0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057   -1.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6182   -1.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0946    0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9071    1.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1893    1.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4374    0.4298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    2.2150    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  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  9 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 18 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 27  1  0  0  0  0
M  END

     RDKit          3D

 63 63  0  0  0  0  0  0  0  0999 V2000
    5.6769   -0.6476   -0.4214 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8815   -1.7443    0.1959 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.5671   -3.0378    0.4584 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6035   -1.5915    0.5083 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9592   -0.3081    0.2378 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7901   -0.3763   -0.6986 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.1872   -0.7688   -1.9706 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.7091   -1.3241   -0.2357 C   0  0  2  0  0  0  0  0  0  0  0  0
    1.1421   -2.6201   -0.5064 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5469   -0.9646   -0.9406 C   0  0  1  0  0  0  0  0  0  0  0  0
   -0.3601   -0.7214   -2.3054 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6504   -1.9796   -0.8141 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9680   -2.3438    0.5653 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1874   -2.1429    1.0423 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2560   -1.5470    0.1950 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.5237   -2.5160    2.4657 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0733    0.3403   -0.3239 C   0  0  2  0  0  0  0  0  0  0  0  0
   -1.9819    0.9001   -1.1913 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0376    1.2567    0.0266 C   0  0  2  0  0  0  0  0  0  0  0  0
    0.4413    1.0870    1.3548 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3552    2.7182   -0.0881 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4706    3.1056    0.7841 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5474    3.7147    0.3528 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.7124    4.0612   -1.0649 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6515    4.0754    1.3167 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2684    1.0586   -0.8438 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.2191    1.9834   -0.4117 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.2117   -0.2882   -1.3860 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.6696    0.2383    0.2526 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.6939   -0.9894   -0.6283 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.3486   -3.2023   -0.2907 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8401   -3.8663    0.5538 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0688   -2.9214    1.4555 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.1083   -2.4506    0.9552 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.6585    0.1570    1.1990 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.6963    0.3820   -0.2109 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9286   -1.7089   -2.1497 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5510   -1.1740    0.8644 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4158   -3.2574   -0.6385 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4255   -1.5871   -2.7572 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.5502   -1.5199   -1.2725 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4520   -2.8910   -1.4432 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2153   -2.7816    1.2161 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0672   -0.5060   -0.0864 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2299   -1.5887    0.7216 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.4108   -2.1566   -0.7392 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.6002   -2.7985    2.9881 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1737   -3.4304    2.4082 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1133   -1.7337    2.9571 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5925   -0.0084    0.6193 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7265    0.6284   -2.1187 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8392    1.9175    1.7190 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5140    3.3743    0.2056 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5096    2.9597   -1.1670 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3895    2.8709    1.8388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.1939    3.2555   -1.6483 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4566    4.9196   -1.1447 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7788    4.4342   -1.5516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7739    3.1935    1.9809 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5757    4.3143    0.7857 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3282    4.9526    1.9011 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.0430    1.2995   -1.9040 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7780    2.2961   -1.1722 H   0  0  0  0  0  0  0  0  0  0  0  0
 15 14  1  0
 14 16  1  0
 14 13  2  3
 13 12  1  0
 12 10  1  0
 10 11  1  6
 10 17  1  0
 17 18  1  0
 17 19  1  0
 19 20  1  1
 19 21  1  0
 21 22  1  0
 22 23  2  3
 23 24  1  0
 23 25  1  0
 19 26  1  0
 26 27  1  0
 26  6  1  0
  6  7  1  6
  6  5  1  0
  5  4  1  0
  4  2  2  3
  2  1  1  0
  2  3  1  0
  6  8  1  0
  8  9  1  0
  8 10  1  0
 15 44  1  0
 15 45  1  0
 15 46  1  0
 16 47  1  0
 16 48  1  0
 16 49  1  0
 13 43  1  0
 12 41  1  0
 12 42  1  0
 11 40  1  0
 17 50  1  1
 18 51  1  0
 20 52  1  0
 21 53  1  0
 21 54  1  0
 22 55  1  0
 24 56  1  0
 24 57  1  0
 24 58  1  0
 25 59  1  0
 25 60  1  0
 25 61  1  0
 26 62  1  6
 27 63  1  0
  7 37  1  0
  5 35  1  0
  5 36  1  0
  4 34  1  0
  1 28  1  0
  1 29  1  0
  1 30  1  0
  3 31  1  0
  3 32  1  0
  3 33  1  0
  8 38  1  1
  9 39  1  0
M  END


  Mrv1533004231522272D          

 27 27  0  0  0  0            999 V2000
    2.3054    3.1335    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5875    2.3582    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.0572    1.7262    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2448    1.8695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145    1.2375    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1842    1.8695    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.1434    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4289   -0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2414    0.1433    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.7111   -0.7752    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5236   -0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8057   -1.6938    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6182   -1.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2754   -2.3257    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -0.4125    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7145   -1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.0000    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2822   -0.7752    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8125    0.1433    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0946    0.9185    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9071    1.0618    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1893    1.8370    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4374    0.4298    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0000    0.8250    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.7145    1.2375    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.4000    2.2150    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  1  0  0  0  0
  5  6  1  0  0  0  0
  5  7  1  0  0  0  0
  7  8  1  0  0  0  0
  7  9  1  0  0  0  0
  9 10  1  0  0  0  0
  9 11  1  0  0  0  0
 11 12  1  0  0  0  0
 12 13  2  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
  9 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
 18 20  1  0  0  0  0
 20 21  1  0  0  0  0
 21 22  2  0  0  0  0
 22 23  1  0  0  0  0
 22 24  1  0  0  0  0
 18 25  1  0  0  0  0
  5 25  1  0  0  0  0
 25 26  1  0  0  0  0
  2 27  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0181849

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CC(C)=CCC1(O)C(O)C(O)(CC=C(C)C)C(O)C(O)(CC=C(C)C)C1O

> <INCHI_IDENTIFIER>
InChI=1S/C21H36O6/c1-13(2)7-10-19(25)16(22)20(26,11-8-14(3)4)18(24)21(27,17(19)23)12-9-15(5)6/h7-9,16-18,22-27H,10-12H2,1-6H3

> <INCHI_KEY>
GASLMESBWZWBPN-UHFFFAOYSA-N

> <FORMULA>
C21H36O6

> <MOLECULAR_WEIGHT>
384.513

> <EXACT_MASS>
384.251188879

> <JCHEM_ACCEPTOR_COUNT>
6

> <JCHEM_ATOM_COUNT>
63

> <JCHEM_AVERAGE_POLARIZABILITY>
42.558736582008265

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
6

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol

> <ALOGPS_LOGP>
0.85

> <JCHEM_LOGP>
0.9390183730000001

> <ALOGPS_LOGS>
-2.27

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
12.545875452458219

> <JCHEM_PKA_STRONGEST_ACIDIC>
11.930970044591199

> <JCHEM_PKA_STRONGEST_BASIC>
-3.7822415503789317

> <JCHEM_POLAR_SURFACE_AREA>
121.38000000000001

> <JCHEM_REFRACTIVITY>
107.06339999999997

> <JCHEM_ROTATABLE_BOND_COUNT>
6

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
2.05e+00 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 23-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   23-APR-15         0                                  
HETATM    1  C   UNK     0       4.303   5.849   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0       4.830   4.402   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       3.840   3.222   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0       2.324   3.490   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       1.334   2.310   0.000  0.00  0.00           C+0
HETATM    6  O   UNK     0       0.344   3.490   0.000  0.00  0.00           O+0
HETATM    7  C   UNK     0       2.667   1.540   0.000  0.00  0.00           C+0
HETATM    8  O   UNK     0       4.001   2.310   0.000  0.00  0.00           O+0
HETATM    9  C   UNK     0       2.667  -0.000   0.000  0.00  0.00           C+0
HETATM   10  O   UNK     0       4.184   0.267   0.000  0.00  0.00           O+0
HETATM   11  C   UNK     0       3.194  -1.447   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       4.711  -1.715   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       5.237  -3.162   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       6.754  -3.429   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       4.247  -4.341   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       1.334  -0.770   0.000  0.00  0.00           C+0
HETATM   17  O   UNK     0       1.334  -2.310   0.000  0.00  0.00           O+0
HETATM   18  C   UNK     0       0.000   0.000   0.000  0.00  0.00           C+0
HETATM   19  O   UNK     0      -0.527  -1.447   0.000  0.00  0.00           O+0
HETATM   20  C   UNK     0      -1.517   0.267   0.000  0.00  0.00           C+0
HETATM   21  C   UNK     0      -2.043   1.715   0.000  0.00  0.00           C+0
HETATM   22  C   UNK     0      -3.560   1.982   0.000  0.00  0.00           C+0
HETATM   23  C   UNK     0      -4.087   3.429   0.000  0.00  0.00           C+0
HETATM   24  C   UNK     0      -4.550   0.802   0.000  0.00  0.00           C+0
HETATM   25  C   UNK     0       0.000   1.540   0.000  0.00  0.00           C+0
HETATM   26  O   UNK     0      -1.334   2.310   0.000  0.00  0.00           O+0
HETATM   27  C   UNK     0       6.347   4.135   0.000  0.00  0.00           C+0
CONECT    1    2                                                            
CONECT    2    1    3   27                                                  
CONECT    3    2    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6    7   25                                             
CONECT    6    5                                                            
CONECT    7    5    8    9                                                  
CONECT    8    7                                                            
CONECT    9    7   10   11   16                                             
CONECT   10    9                                                            
CONECT   11    9   12                                                       
CONECT   12   11   13                                                       
CONECT   13   12   14   15                                                  
CONECT   14   13                                                            
CONECT   15   13                                                            
CONECT   16    9   17   18                                                  
CONECT   17   16                                                            
CONECT   18   16   19   20   25                                             
CONECT   19   18                                                            
CONECT   20   18   21                                                       
CONECT   21   20   22                                                       
CONECT   22   21   23   24                                                  
CONECT   23   22                                                            
CONECT   24   22                                                            
CONECT   25   18    5   26                                                  
CONECT   26   25                                                            
CONECT   27    2                                                            
MASTER        0    0    0    0    0    0    0    0   27    0   54    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₃₆O₆

Average Mass

384.5130 Da

Monoisotopic Mass

384.25119 Da

IUPAC Name

1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol

Traditional Name

1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol

CAS Registry Number

Not Available

SMILES

CC(C)=CCC1(O)C(O)C(O)(CC=C(C)C)C(O)C(O)(CC=C(C)C)C1O

InChI Identifier

InChI=1S/C21H36O6/c1-13(2)7-10-19(25)16(22)20(26,11-8-14(3)4)18(24)21(27,17(19)23)12-9-15(5)6/h7-9,16-18,22-27H,10-12H2,1-6H3

InChI Key

GASLMESBWZWBPN-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

Species Name	Source	Reference
Evodiella muelleri	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as cyclohexanols. Cyclohexanols are compounds containing an alcohol group attached to a cyclohexane ring.

Kingdom

Organic compounds

Super Class

Organic oxygen compounds

Class

Organooxygen compounds

Sub Class

Alcohols and polyols

Direct Parent

Cyclohexanols

Alternative Parents

Substituents

Cyclohexanol
Sugar alcohol
Cyclitol or derivatives
Tertiary alcohol
Cyclic alcohol
Polyol
Hydrocarbon derivative
Aliphatic homomonocyclic compound

Molecular Framework

Aliphatic homomonocyclic 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	0.85	ALOGPS
logP	0.94	ChemAxon
logS	-2.3	ALOGPS
pKa (Strongest Acidic)	11.93	ChemAxon
pKa (Strongest Basic)	-3.8	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	6	ChemAxon
Hydrogen Donor Count	6	ChemAxon
Polar Surface Area	121.38 Å²	ChemAxon
Rotatable Bond Count	6	ChemAxon
Refractivity	107.06 m³·mol⁻¹	ChemAxon
Polarizability	42.56 Å³	ChemAxon
Number of Rings	1	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

101324822

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for 1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol (NP0181849)

MOL for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

3D MOL for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

3D SDF for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

3D-SDF for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

PDB for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

3D PDB for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

SMILES for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

INCHI for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

Structure for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)

3D Structure for NP0181849 (1,3,5-tris(3-methylbut-2-en-1-yl)cyclohexane-1,2,3,4,5,6-hexol)