NP-MRD: Showing NP-Card for [6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid (NP0171969)

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Record Information

Version

2.0

Created at

2022-09-03 08:42:35 UTC

Updated at

2022-09-03 08:42:36 UTC

NP-MRD ID

NP0171969

Secondary Accession Numbers

None

Natural Product Identification

Common Name

[6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid

Description

2-[6-(2,4-Dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid belongs to the class of organic compounds known as 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2. 2-[6-(2,4-Dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid is an extremely weak basic (essentially neutral) compound (based on its pKa).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 60 60  0  0  0  0  0  0  0  0999 V2000
    5.7703    1.9105   -0.2476 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.7541    0.4678    0.2222 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.8790    0.2803    1.4413 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.4604    0.6571    1.2060 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.7762   -0.1151    0.1300 C   0  0  1  0  0  0  0  0  0  0  0  0
    2.6901   -1.5797    0.3116 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.3597    0.4538   -0.0088 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5582   -0.2248   -1.0343 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0981   -0.2688   -2.4707 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6049   -0.8192   -0.8658 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4009   -0.9565    0.3701 C   0  0  2  0  0  0  0  0  0  0  0  0
   -0.8778   -2.0540    1.2082 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8852   -3.4029    0.5369 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8572   -1.1044   -0.0011 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6725    0.1392    0.0577 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.6813    0.1251    1.1906 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.0652   -0.0103    2.5530 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9142    1.3995   -0.0492 C   0  0  2  0  0  0  0  0  0  0  0  0
   -2.8307    1.9538   -1.4746 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1712    2.2564   -2.0039 C   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2187    2.1330   -1.3220 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3579    2.7066   -3.3197 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.6162    1.2628    0.3842 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3418    0.2436    1.1223 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.7711    2.1995   -0.6212 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.5496    1.9945   -1.0294 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.0069    2.6060    0.5833 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.3658   -0.1594   -0.5940 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.8056    0.2023    0.4422 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.0345   -0.7335    1.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
    5.2843    0.9828    2.2187 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.8896    0.5516    2.1372 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.4375    1.7304    0.9088 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.3514    0.0681   -0.8116 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.5626   -1.8493    1.3762 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7869   -1.9403   -0.2628 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.5391   -2.1509   -0.1133 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.4761    1.5362   -0.2261 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.9092    0.3623    0.9723 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.0492    0.2565   -2.5267 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2666   -1.3511   -2.6516 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3725    0.1828   -3.1576 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0441   -1.2793   -1.7697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4142   -2.1609    2.1915 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.1591   -1.8363    1.5051 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8540   -4.1672    1.3407 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7766   -3.5921   -0.0660 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0464   -3.5782   -0.0697 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3659   -1.8857    0.6069 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8779   -1.5034   -1.0358 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.3323    0.0958   -0.8763 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.4210   -0.6921    1.0516 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.2709    1.0646    1.2011 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8300   -0.1980    3.3337 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4040   -0.9002    2.5269 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4135    0.8552    2.8061 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.3990    2.2477    0.5206 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4397    1.0912   -2.0910 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.1456    2.8032   -1.5067 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.5262    3.6936   -3.4489 H   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0
  2  3  1  0
  3  4  1  0
  4  5  1  0
  5  6  1  0
  5  7  1  0
  7  8  1  0
  8  9  1  0
  8 10  2  0
 11 10  1  6
 11 12  1  0
 12 13  1  0
 11 14  1  0
 14 15  1  0
 15 16  1  0
 16 17  1  0
 15 18  1  0
 18 19  1  0
 19 20  1  0
 20 22  1  0
 20 21  2  0
 18 23  1  0
 23 24  1  0
 24 11  1  0
  1 25  1  0
  1 26  1  0
  1 27  1  0
  2 28  1  0
  2 29  1  0
  3 30  1  0
  3 31  1  0
  4 32  1  0
  4 33  1  0
  5 34  1  6
  6 35  1  0
  6 36  1  0
  6 37  1  0
  7 38  1  0
  7 39  1  0
  9 40  1  0
  9 41  1  0
  9 42  1  0
 10 43  1  0
 12 44  1  0
 12 45  1  0
 13 46  1  0
 13 47  1  0
 13 48  1  0
 14 49  1  0
 14 50  1  0
 15 51  1  6
 16 52  1  0
 16 53  1  0
 17 54  1  0
 17 55  1  0
 17 56  1  0
 18 57  1  1
 19 58  1  0
 19 59  1  0
 22 60  1  0
M  END


  Mrv1533004181500282D          

 24 24  0  0  0  0            999 V2000
   -2.1212   -3.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4067   -2.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4067   -2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6923   -1.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0222   -2.1154    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7367   -1.7029    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0222   -2.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7367   -3.3529    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.7367   -4.1779    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512   -4.5904    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.9209   -5.2224    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2030   -5.9977    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7333   -3.8152    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5458   -3.6719    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8280   -2.8967    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.6404   -2.7534    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.0761   -4.3039    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8886   -4.1607    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.4189   -4.7927    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2313   -4.6494    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.1367   -5.5679    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.7939   -5.0792    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.9815   -5.2224    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.4512   -2.9404    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  1  0  0  0  0
  2  3  1  0  0  0  0
  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
  8  9  2  0  0  0  0
  9 10  1  4  0  0  0
 10 11  1  0  0  0  0
 11 12  1  0  0  0  0
 10 13  1  0  0  0  0
 13 14  1  0  0  0  0
 14 15  1  0  0  0  0
 15 16  1  0  0  0  0
 14 17  1  0  0  0  0
 17 18  1  0  0  0  0
 18 19  1  0  0  0  0
 19 20  2  0  0  0  0
 19 21  1  0  0  0  0
 17 22  1  0  0  0  0
 22 23  1  0  0  0  0
 10 23  1  0  0  0  0
  8 24  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0171969

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCC(C)CC(C)=CC1(CC)CC(CC)C(CC(O)=O)OO1

> <INCHI_IDENTIFIER>
InChI=1S/C20H36O4/c1-6-9-10-15(4)11-16(5)13-20(8-3)14-17(7-2)18(23-24-20)12-19(21)22/h13,15,17-18H,6-12,14H2,1-5H3,(H,21,22)

> <INCHI_KEY>
IVJFFFBKADEWIF-UHFFFAOYSA-N

> <FORMULA>
C20H36O4

> <MOLECULAR_WEIGHT>
340.504

> <EXACT_MASS>
340.261359639

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
60

> <JCHEM_AVERAGE_POLARIZABILITY>
40.36083960942484

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
1

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
0

> <JCHEM_IUPAC>
2-[6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid

> <ALOGPS_LOGP>
5.66

> <JCHEM_LOGP>
6.032795748333333

> <ALOGPS_LOGS>
-4.56

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
-1

> <JCHEM_PKA_STRONGEST_ACIDIC>
4.588627906703993

> <JCHEM_PKA_STRONGEST_BASIC>
-4.855075104245575

> <JCHEM_POLAR_SURFACE_AREA>
55.760000000000005

> <JCHEM_REFRACTIVITY>
96.6658

> <JCHEM_ROTATABLE_BOND_COUNT>
10

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
9.44e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
[6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid

> <JCHEM_VEBER_RULE>
0

$$$$

HEADER    PROTEIN                                 18-APR-15   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   18-APR-15         0                                  
HETATM    1  C   UNK     0      -3.960  -6.259   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.626  -5.489   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0      -2.626  -3.949   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.292  -3.179   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       0.041  -3.949   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.375  -3.179   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       0.041  -5.489   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       1.375  -6.259   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       1.375  -7.799   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       2.709  -8.569   0.000  0.00  0.00           C+0
HETATM   11  C   UNK     0       1.719  -9.749   0.000  0.00  0.00           C+0
HETATM   12  C   UNK     0       2.246 -11.196   0.000  0.00  0.00           C+0
HETATM   13  C   UNK     0       3.236  -7.122   0.000  0.00  0.00           C+0
HETATM   14  C   UNK     0       4.752  -6.854   0.000  0.00  0.00           C+0
HETATM   15  C   UNK     0       5.279  -5.407   0.000  0.00  0.00           C+0
HETATM   16  C   UNK     0       6.795  -5.140   0.000  0.00  0.00           C+0
HETATM   17  C   UNK     0       5.742  -8.034   0.000  0.00  0.00           C+0
HETATM   18  C   UNK     0       7.259  -7.767   0.000  0.00  0.00           C+0
HETATM   19  C   UNK     0       8.249  -8.946   0.000  0.00  0.00           C+0
HETATM   20  O   UNK     0       9.765  -8.679   0.000  0.00  0.00           O+0
HETATM   21  O   UNK     0       7.722 -10.393   0.000  0.00  0.00           O+0
HETATM   22  O   UNK     0       5.215  -9.481   0.000  0.00  0.00           O+0
HETATM   23  O   UNK     0       3.699  -9.749   0.000  0.00  0.00           O+0
HETATM   24  C   UNK     0       2.709  -5.489   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    7                                                  
CONECT    6    5                                                            
CONECT    7    5    8                                                       
CONECT    8    7    9   24                                                  
CONECT    9    8   10                                                       
CONECT   10    9   11   13   23                                             
CONECT   11   10   12                                                       
CONECT   12   11                                                            
CONECT   13   10   14                                                       
CONECT   14   13   15   17                                                  
CONECT   15   14   16                                                       
CONECT   16   15                                                            
CONECT   17   14   18   22                                                  
CONECT   18   17   19                                                       
CONECT   19   18   20   21                                                  
CONECT   20   19                                                            
CONECT   21   19                                                            
CONECT   22   17   23                                                       
CONECT   23   22   10                                                       
CONECT   24    8                                                            
MASTER        0    0    0    0    0    0    0    0   24    0   48    0
END

View in JSmol

Synonyms

Value	Source
2-[6-(2,4-Dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetate	Generator

Chemical Formula

C₂₀H₃₆O₄

Average Mass

340.5040 Da

Monoisotopic Mass

340.26136 Da

IUPAC Name

2-[6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid

Traditional Name

[6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid

CAS Registry Number

Not Available

SMILES

CCCCC(C)CC(C)=CC1(CC)CC(CC)C(CC(O)=O)OO1

InChI Identifier

InChI=1S/C20H36O4/c1-6-9-10-15(4)11-16(5)13-20(8-3)14-17(7-2)18(23-24-20)12-19(21)22/h13,15,17-18H,6-12,14H2,1-5H3,(H,21,22)

InChI Key

IVJFFFBKADEWIF-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 1,2-dioxanes. These are organic compounds containing 1,2-dioxane, an aliphatic six-member ring with two oxygen atoms in ring positions 1 and 2.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxanes

Sub Class

1,2-dioxanes

Direct Parent

1,2-dioxanes

Alternative Parents

Substituents

Ortho-dioxane
Dialkyl peroxide
Oxacycle
Monocarboxylic acid or derivatives
Carboxylic acid
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic heteromonocyclic compound

Molecular Framework

Aliphatic heteromonocyclic 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	5.66	ALOGPS
logP	6.03	ChemAxon
logS	-4.6	ALOGPS
pKa (Strongest Acidic)	4.59	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	-1	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	1	ChemAxon
Polar Surface Area	55.76 Å²	ChemAxon
Rotatable Bond Count	10	ChemAxon
Refractivity	96.67 m³·mol⁻¹	ChemAxon
Polarizability	40.36 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	No	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

73803333

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for [6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid (NP0171969)

MOL for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

3D MOL for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

3D SDF for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

3D-SDF for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

PDB for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

3D PDB for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

SMILES for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

INCHI for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

Structure for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)

3D Structure for NP0171969 ([6-(2,4-dimethyloct-1-en-1-yl)-4,6-diethyl-1,2-dioxan-3-yl]acetic acid)