NP-MRD: Showing NP-Card for 4-Methyl-2-nonyl-1,3-dioxolane (NP0044911)

Jump To Section:

Identification Spectra BioTaxonomy ChemoTaxonomy Physical properties Links References XML

Record Information

Version

2.0

Created at

2022-03-10 18:50:58 UTC

Updated at

2022-03-10 22:17:29 UTC

NP-MRD ID

NP0044911

Secondary Accession Numbers

None

Natural Product Identification

Common Name

4-Methyl-2-nonyl-1,3-dioxolane

Description

Decanal propyleneglycol acetal, also known as decanal or 4-methyl-2-nonyl-1,3-dioxolane, belongs to the class of organic compounds known as 1,3-dioxolanes. These are organic compounds containing 1,3-dioxolane, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 3. Decanal propyleneglycol acetal is a neutral compound, a colorless clear liquid with a floral, green herbal odor ( http://Www.Thegoodscentscompany.Com/data/rw1383421.Html#toorgano). Decanal propyleneglycol acetal is found in cannabis plants (PMID:6991645 ).

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 41 41  0  0  0  0  0  0  0  0999 V2000
    5.3842    0.9913   -1.0530 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2120    1.1451    0.4224 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.3666    0.0466    1.0287 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9717    0.0260    0.4205 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.2359   -1.0985    1.0994 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.8240   -1.3004    0.6249 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.0308   -0.0689    0.8757 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4121   -0.1841    0.4439 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5690   -0.4638   -1.0084 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0284   -0.5713   -1.4360 C   0  0  1  0  0  0  0  0  0  0  0  0
   -3.7167   -1.5727   -0.7882 O   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6065   -0.9177    0.0382 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9564    0.3194   -0.7840 C   0  0  1  0  0  0  0  0  0  0  0  0
   -5.4620    1.4268    0.0860 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.6936    0.6229   -1.3221 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.1422   -0.0415   -1.3870 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7070    1.6742   -1.6091 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.4086    1.2555   -1.3289 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7370    2.1228    0.6427 H   0  0  0  0  0  0  0  0  0  0  0  0
    6.2069    1.0827    0.9097 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.8148   -0.9397    0.8845 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.2494    0.2937    2.1035 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.4815    1.0086    0.5632 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.0783   -0.1489   -0.6608 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.2274   -0.9020    2.2137 H   0  0  0  0  0  0  0  0  0  0  0  0
    2.7767   -2.0661    1.0097 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8858   -1.5492   -0.4646 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4099   -2.2001    1.1389 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.0613    0.1604    1.9594 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.5276    0.7825    0.3316 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9258    0.7459    0.7519 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8841   -1.0179    1.0059 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9948   -1.3104   -1.3788 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1780    0.4405   -1.5614 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0260   -0.8656   -2.5253 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.5636   -1.4929    0.1323 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.2372   -0.6592    1.0327 H   0  0  0  0  0  0  0  0  0  0  0  0
   -5.6917    0.1077   -1.5620 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.1569    0.9924    0.8336 H   0  0  0  0  0  0  0  0  0  0  0  0
   -6.0215    2.1587   -0.5324 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6154    1.9673    0.5569 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
  6  7  1  0
  7  8  1  0
  8  9  1  0
  9 10  1  0
 10 11  1  0
 11 12  1  0
 12 13  1  0
 13 14  1  0
 13 15  1  0
 15 10  1  0
  1 16  1  0
  1 17  1  0
  1 18  1  0
  2 19  1  0
  2 20  1  0
  3 21  1  0
  3 22  1  0
  4 23  1  0
  4 24  1  0
  5 25  1  0
  5 26  1  0
  6 27  1  0
  6 28  1  0
  7 29  1  0
  7 30  1  0
  8 31  1  0
  8 32  1  0
  9 33  1  0
  9 34  1  0
 10 35  1  6
 12 36  1  0
 12 37  1  0
 13 38  1  6
 14 39  1  0
 14 40  1  0
 14 41  1  0
M  END


  Mrv1652303192000273D          

 15 15  0  0  0  0            999 V2000
    5.0818    1.7752   -0.9004 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.7057    1.7101   -0.8885 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.9985    0.8037    0.2567 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5141    0.5108    0.4800 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.9459   -0.0899   -0.7729 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.4750   -0.3662   -0.6046 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.2580   -1.3360    0.5097 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2176   -1.6637    0.6315 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.9912   -0.4235    0.9256 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.4643   -0.7217    1.1117 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.9597   -0.3047   -0.0659 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.1468    0.2976   -1.1639 C   0  0  2  0  0  0  0  0  0  0  0  0
   -3.0419   -1.3247   -0.1149 C   0  0  1  0  0  0  0  0  0  0  0  0
   -4.4056   -1.5678    0.1123 O   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0392   -0.5134   -1.2183 O   0  0  0  0  0  0  0  0  0  0  0  0
  1  3  1  0  0  0  0
  2 12  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
  6  7  1  0  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 13  1  0  0  0  0
 11 12  1  0  0  0  0
 11 14  1  0  0  0  0
 12 15  1  0  0  0  0
 13 14  1  0  0  0  0
 13 15  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0044911

> <DATABASE_NAME>
NP-MRD

> <SMILES>
CCCCCCCCC[C@H]1OC[C@@H](C)O1

> <INCHI_IDENTIFIER>
InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-13-14-11-12(2)15-13/h12-13H,3-11H2,1-2H3/t12-,13+/m1/s1

> <INCHI_KEY>
SJLDHKPBFAHHSI-OLZOCXBDSA-N

> <FORMULA>
C13H26O2

> <MOLECULAR_WEIGHT>
214.349

> <EXACT_MASS>
214.193280077

> <JCHEM_ACCEPTOR_COUNT>
2

> <JCHEM_ATOM_COUNT>
41

> <JCHEM_AVERAGE_POLARIZABILITY>
27.779617786417013

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
0

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
(2S,4R)-4-methyl-2-nonyl-1,3-dioxolane

> <ALOGPS_LOGP>
4.22

> <JCHEM_LOGP>
4.411111617

> <ALOGPS_LOGS>
-4.30

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
1

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA_STRONGEST_BASIC>
-4.042878951001777

> <JCHEM_POLAR_SURFACE_AREA>
18.46

> <JCHEM_REFRACTIVITY>
62.83340000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
8

> <JCHEM_RULE_OF_FIVE>
1

> <ALOGPS_SOLUBILITY>
1.06e-02 g/l

> <JCHEM_TRADITIONAL_IUPAC>
(2S,4R)-4-methyl-2-nonyl-1,3-dioxolane

> <JCHEM_VEBER_RULE>
1

$$$$

HEADER    PROTEIN                                 19-MAR-20   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   19-MAR-20         0                                  
HETATM    1  C   UNK     0       5.082   1.775  -0.900  0.00  0.00           C+0
HETATM    2  C   UNK     0      -3.706   1.710  -0.889  0.00  0.00           C+0
HETATM    3  C   UNK     0       4.999   0.804   0.257  0.00  0.00           C+0
HETATM    4  C   UNK     0       3.514   0.511   0.480  0.00  0.00           C+0
HETATM    5  C   UNK     0       2.946  -0.090  -0.773  0.00  0.00           C+0
HETATM    6  C   UNK     0       1.475  -0.366  -0.605  0.00  0.00           C+0
HETATM    7  C   UNK     0       1.258  -1.336   0.510  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.218  -1.664   0.632  0.00  0.00           C+0
HETATM    9  C   UNK     0      -0.991  -0.424   0.926  0.00  0.00           C+0
HETATM   10  C   UNK     0      -2.464  -0.722   1.112  0.00  0.00           C+0
HETATM   11  C   UNK     0      -4.960  -0.305  -0.066  0.00  0.00           C+0
HETATM   12  C   UNK     0      -4.147   0.298  -1.164  0.00  0.00           C+0
HETATM   13  C   UNK     0      -3.042  -1.325  -0.115  0.00  0.00           C+0
HETATM   14  O   UNK     0      -4.406  -1.568   0.112  0.00  0.00           O+0
HETATM   15  O   UNK     0      -3.039  -0.513  -1.218  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2   12                                                            
CONECT    3    1    4                                                       
CONECT    4    3    5                                                       
CONECT    5    4    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   13                                                       
CONECT   11   12   14                                                       
CONECT   12    2   11   15                                                  
CONECT   13   10   14   15                                                  
CONECT   14   11   13                                                       
CONECT   15   12   13                                                       
MASTER        0    0    0    0    0    0    0    0   15    0   30    0
END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₁₃H₂₆O₂

Average Mass

214.3490 Da

Monoisotopic Mass

214.19328 Da

IUPAC Name

(2S,4R)-4-methyl-2-nonyl-1,3-dioxolane

Traditional Name

(2S,4R)-4-methyl-2-nonyl-1,3-dioxolane

CAS Registry Number

5421-12-5

SMILES

CCCCCCCCC[C@H]1OC[C@@H](C)O1

InChI Identifier

InChI=1S/C13H26O2/c1-3-4-5-6-7-8-9-10-13-14-11-12(2)15-13/h12-13H,3-11H2,1-2H3/t12-,13+/m1/s1

InChI Key

SJLDHKPBFAHHSI-OLZOCXBDSA-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, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 252 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 50 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 75 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 101 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 126 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 151 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 176 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 201 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 226 MHz, D₂O, predicted)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, D₂O, 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
Cannabis sativa	NULL	Not Available

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as 1,3-dioxolanes. These are organic compounds containing 1,3-dioxolane, an aliphatic five-member ring with two oxygen atoms in ring positions 1 and 3.

Kingdom

Organic compounds

Super Class

Organoheterocyclic compounds

Class

Dioxolanes

Sub Class

1,3-dioxolanes

Direct Parent

1,3-dioxolanes

Alternative Parents

Substituents

Meta-dioxolane
Oxacycle
Acetal
Organic oxygen compound
Hydrocarbon derivative
Organooxygen compound
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	4.22	ALOGPS
logP	4.41	ChemAxon
logS	-4.3	ALOGPS
pKa (Strongest Basic)	-4	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	2	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	18.46 Å²	ChemAxon
Rotatable Bond Count	8	ChemAxon
Refractivity	62.83 m³·mol⁻¹	ChemAxon
Polarizability	27.78 Å³	ChemAxon
Number of Rings	1	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	Yes	ChemAxon
Ghose Filter	Yes	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

76959550

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

Showing NP-Card for 4-Methyl-2-nonyl-1,3-dioxolane (NP0044911)

MOL for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

3D MOL for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

3D SDF for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

3D-SDF for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

PDB for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

3D PDB for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

SMILES for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

INCHI for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

Structure for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)

3D Structure for NP0044911 (4-Methyl-2-nonyl-1,3-dioxolane)