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

Details

Stereochemistry ACHIRAL
Molecular Formula C5H11NO
Molecular Weight 101.1469
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VALERAMIDE

SMILES

CCCCC(N)=O

InChI

InChIKey=IPWFJLQDVFKJDU-UHFFFAOYSA-N
InChI=1S/C5H11NO/c1-2-3-4-5(6)7/h2-4H2,1H3,(H2,6,7)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
A new acylamidase from Rhodococcus erythropolis TA37 can hydrolyze N-substituted amides.
2010 Aug
Redetermination of 5α-androstane-3,17-dione.
2010 May 29
Patents
Name Type Language
VALERAMIDE
Systematic Name English
VALPROIC ACID IMPURITY E [EP IMPURITY]
Common Name English
N-VALERAMIDE
Common Name English
NSC-400223
Code English
PENTANAMIDE
Systematic Name English
PENTANIMIDIC ACID
Systematic Name English
VALERIC ACID AMIDE
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID3060827
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
FDA UNII
TKL9TN43QK
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
CAS
626-97-1
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
NSC
400223
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
CHEBI
16459
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
PUBCHEM
12298
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
MESH
C055998
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY
ECHA (EC/EINECS)
210-974-0
Created by admin on Fri Dec 15 19:48:14 GMT 2023 , Edited by admin on Fri Dec 15 19:48:14 GMT 2023
PRIMARY