NP-MRD: Showing NP-Card for (3e)-ethyl 3-octenoate (NP0204025)

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Record Information

Version

2.0

Created at

2022-09-04 23:37:23 UTC

Updated at

2022-09-04 23:37:23 UTC

NP-MRD ID

NP0204025

Secondary Accession Numbers

None

Natural Product Identification

Common Name

(3e)-ethyl 3-octenoate

Description

Ethyl 3-octenoate belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid. Ethyl 3-octenoate is a very hydrophobic molecule, practically insoluble (in water), and relatively neutral. Ethyl 3-octenoate is a fruity and tropical tasting compound. (3e)-ethyl 3-octenoate is found in Ceratitis capitata. Outside of the human body,.

Structure

MOL 3D MOL SDF PDB SMILES InChI

     RDKit          3D

 30 29  0  0  0  0  0  0  0  0999 V2000
   -4.1773   -0.2156    0.6038 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8640    0.0931    1.3327 C   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2386    1.2599    0.6284 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9555    0.9543   -0.8240 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.0230   -0.1937   -0.9496 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1506   -0.0271   -1.5625 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.0663   -1.1765   -1.6797 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.3722   -0.9091   -1.0078 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2474   -1.7993   -1.0282 O   0  0  0  0  0  0  0  0  0  0  0  0
    2.6402    0.2738   -0.3734 O   0  0  0  0  0  0  0  0  0  0  0  0
    3.8562    0.5791    0.2771 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.1633   -0.3748    1.3983 C   0  0  0  0  0  0  0  0  0  0  0  0
   -4.8265   -0.7077    1.3659 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.9633   -0.8999   -0.2490 H   0  0  0  0  0  0  0  0  0  0  0  0
   -4.6798    0.6915    0.2548 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.2215   -0.8066    1.2593 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0675    0.3064    2.4017 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.8762    2.1518    0.7256 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2663    1.4734    1.1575 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5159    1.8823   -1.2588 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.9427    0.7275   -1.2970 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.3314   -1.1476   -0.5331 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.3669    0.9611   -1.9457 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.2210   -1.3907   -2.7751 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.6094   -2.0952   -1.2614 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7773    1.6247    0.6525 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7186    0.5726   -0.4252 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.2593   -0.7773    1.8839 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7787   -1.2294    1.0582 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.7220    0.1992    2.1707 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  2  0
  6  7  1  0
  7  8  1  0
  8  9  2  0
  8 10  1  0
 10 11  1  0
 11 12  1  0
  1 13  1  0
  1 14  1  0
  1 15  1  0
  2 16  1  0
  2 17  1  0
  3 18  1  0
  3 19  1  0
  4 20  1  0
  4 21  1  0
  5 22  1  0
  6 23  1  0
  7 24  1  0
  7 25  1  0
 11 26  1  0
 11 27  1  0
 12 28  1  0
 12 29  1  0
 12 30  1  0
M  END

HEADER    PROTEIN                                 06-MAY-13   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   06-MAY-13         0                                  
HETATM    1  C   UNK     0      10.669   0.000   0.000  0.00  0.00           C+0
HETATM    2  C   UNK     0      -2.667   0.000   0.000  0.00  0.00           C+0
HETATM    3  C   UNK     0       9.336   0.770   0.000  0.00  0.00           C+0
HETATM    4  C   UNK     0      -1.334   0.770   0.000  0.00  0.00           C+0
HETATM    5  C   UNK     0       8.002   0.000   0.000  0.00  0.00           C+0
HETATM    6  C   UNK     0       6.668   0.770   0.000  0.00  0.00           C+0
HETATM    7  C   UNK     0       5.335   0.000   0.000  0.00  0.00           C+0
HETATM    8  C   UNK     0       4.001   0.770   0.000  0.00  0.00           C+0
HETATM    9  C   UNK     0       2.667   0.000   0.000  0.00  0.00           C+0
HETATM   10  C   UNK     0       1.334   0.770   0.000  0.00  0.00           C+0
HETATM   11  O   UNK     0       1.334   2.310   0.000  0.00  0.00           O+0
HETATM   12  O   UNK     0       0.000   0.000   0.000  0.00  0.00           O+0
CONECT    1    3                                                            
CONECT    2    4                                                            
CONECT    3    1    5                                                       
CONECT    4    2   12                                                       
CONECT    5    3    6                                                       
CONECT    6    5    7                                                       
CONECT    7    6    8                                                       
CONECT    8    7    9                                                       
CONECT    9    8   10                                                       
CONECT   10    9   11   12                                                  
CONECT   11   10                                                            
CONECT   12    4   10                                                       
MASTER        0    0    0    0    0    0    0    0   12    0   22    0
END

View in JSmol

Synonyms

Value	Source
Ethyl 3-octenoic acid	Generator
Ethyl (3E)-3-octenoate	HMDB
Ethyl oct-3-enoate	HMDB
Ethyl 3E-octenoic acid	Generator

Chemical Formula

C₁₀H₁₈O₂

Average Mass

170.2487 Da

Monoisotopic Mass

170.13068 Da

IUPAC Name

ethyl (3E)-oct-3-enoate

Traditional Name

ethyl (3E)-oct-3-enoate

CAS Registry Number

Not Available

SMILES

CCCC\C=C\CC(=O)OCC

InChI Identifier

InChI=1S/C10H18O2/c1-3-5-6-7-8-9-10(11)12-4-2/h7-8H,3-6,9H2,1-2H3/b8-7+

InChI Key

BCMYNNIPTQUKAC-BQYQJAHWSA-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
Ceratitis capitata	LOTUS Database	35616633

Chemical Taxonomy

Description

Belongs to the class of organic compounds known as fatty acid esters. These are carboxylic ester derivatives of a fatty acid.

Kingdom

Organic compounds

Super Class

Lipids and lipid-like molecules

Class

Fatty Acyls

Sub Class

Fatty acid esters

Direct Parent

Fatty acid esters

Alternative Parents

Substituents

Fatty acid ester
Carboxylic acid ester
Monocarboxylic acid or derivatives
Carboxylic acid derivative
Organic oxygen compound
Organic oxide
Hydrocarbon derivative
Organooxygen compound
Carbonyl group
Aliphatic acyclic compound

Molecular Framework

Aliphatic acyclic compounds

External Descriptors

Wax monoesters (LMFA07010522 )

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	3.47	ALOGPS
logP	2.84	ChemAxon
logS	-3	ALOGPS
pKa (Strongest Basic)	-7.1	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	1	ChemAxon
Hydrogen Donor Count	0	ChemAxon
Polar Surface Area	26.3 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	50.91 m³·mol⁻¹	ChemAxon
Polarizability	20.44 Å³	ChemAxon
Number of Rings	0	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

HMDB0032275

DrugBank ID

Not Available

Phenol Explorer Compound ID

Not Available

FoodDB ID

FDB009404

KNApSAcK ID

Not Available

Chemspider ID

4516553

KEGG Compound ID

Not Available

BioCyc ID

Not Available

BiGG ID

Not Available

Wikipedia Link

Not Available

METLIN ID

Not Available

PubChem Compound

5364397

PDB ID

Not Available

ChEBI ID

Not Available

Good Scents ID

Not Available

References

General References

LOTUS database [Link]

Showing NP-Card for (3e)-ethyl 3-octenoate (NP0204025)

MOL for NP0204025 ((3e)-ethyl 3-octenoate)

3D MOL for NP0204025 ((3e)-ethyl 3-octenoate)

3D SDF for NP0204025 ((3e)-ethyl 3-octenoate)

3D-SDF for NP0204025 ((3e)-ethyl 3-octenoate)

PDB for NP0204025 ((3e)-ethyl 3-octenoate)

3D PDB for NP0204025 ((3e)-ethyl 3-octenoate)

SMILES for NP0204025 ((3e)-ethyl 3-octenoate)

INCHI for NP0204025 ((3e)-ethyl 3-octenoate)

Structure for NP0204025 ((3e)-ethyl 3-octenoate)

3D Structure for NP0204025 ((3e)-ethyl 3-octenoate)