U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C6H9NO2
Molecular Weight 127.1412
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL 3-CYANOPROPANOATE

SMILES

CCOC(=O)CCC#N

InChI

InChIKey=BFSBTNGKMMFQNL-UHFFFAOYSA-N
InChI=1S/C6H9NO2/c1-2-9-6(8)4-3-5-7/h2-4H2,1H3

HIDE SMILES / InChI

Molecular Formula C6H9NO2
Molecular Weight 127.1412
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Crystal structures and solution properties of discrete complexes composed of saddle-distorted molybdenum(v)-dodecaphenylporphyrins and keggin-type heteropolyoxometalates linked by direct coordination.
2010-12-06
Candida albicans-produced farnesol stimulates Pseudomonas quinolone signal production in LasR-defective Pseudomonas aeruginosa strains.
2010-10
Estimation of the ground and the first excited singlet-state dipole moments of 1,4-disubstituted anthraquinone dyes by the solvatochromic method.
2010-04
Pharmacokinetics of cytisine after single intravenous and oral administration in rabbits.
2010-03
Fullerenes for aromatic and non-aromatic N-nitrosamines discrimination.
2009-02-13
Liquid chromatography/fluorescence method for emamectin B1a and desmethylamino-emamectin B1a residues in lobster tissue.
2007-01-18
Simultaneous determination of six HIV protease inhibitors (amprenavir, indinavir, lopinavir, nelfinavir, ritonavir and saquinavir), the active metabolite of nelfinavir (M8) and non-nucleoside reverse transcriptase inhibitor (efavirenz) in human plasma by high-performance liquid chromatography.
2006-01
A peroxyoxalate chemiluminescence-based assay for the evaluation of hydrogen peroxide scavenging activity employing 9,10-diphenylanthracene as the fluorophore.
2004-02-28
Chromium(VI) oxide catalyzed oxidation of sulfides to sulfones with periodic acid.
2003-06-27
Quantitative determination of phenolic diterpenes in rosemary extracts. Aspects of accurate quantification.
2003-05-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:34:22 GMT 2025
Edited
by admin
on Mon Mar 31 19:34:22 GMT 2025
Record UNII
Q745927X6R
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-94973
Preferred Name English
ETHYL 3-CYANOPROPANOATE
Systematic Name English
ETHYL 3-CYANOPROPIONATE
Systematic Name English
PROPIONIC ACID, 3-CYANO-, ETHYL ESTER
Common Name English
3-CYANOPROPANOIC ACID ETHYL ESTER
Systematic Name English
3-CYANOPROPIONIC ACID, ETHYL ESTER
Common Name English
PROPANOIC ACID, 3-CYANO-, ETHYL ESTER
Common Name English
Code System Code Type Description
NSC
94973
Created by admin on Mon Mar 31 19:34:22 GMT 2025 , Edited by admin on Mon Mar 31 19:34:22 GMT 2025
PRIMARY
FDA UNII
Q745927X6R
Created by admin on Mon Mar 31 19:34:22 GMT 2025 , Edited by admin on Mon Mar 31 19:34:22 GMT 2025
PRIMARY
CAS
10137-67-4
Created by admin on Mon Mar 31 19:34:22 GMT 2025 , Edited by admin on Mon Mar 31 19:34:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID10143876
Created by admin on Mon Mar 31 19:34:22 GMT 2025 , Edited by admin on Mon Mar 31 19:34:22 GMT 2025
PRIMARY
PUBCHEM
82393
Created by admin on Mon Mar 31 19:34:22 GMT 2025 , Edited by admin on Mon Mar 31 19:34:22 GMT 2025
PRIMARY