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

Details

Stereochemistry RACEMIC
Molecular Formula C10H13NO
Molecular Weight 163.2163
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-PHENYLBUTYRAMIDE

SMILES

CCC(C(N)=O)C1=CC=CC=C1

InChI

InChIKey=UNFGQCCHVMMMRF-UHFFFAOYSA-N
InChI=1S/C10H13NO/c1-2-9(10(11)12)8-6-4-3-5-7-8/h3-7,9H,2H2,1H3,(H2,11,12)

HIDE SMILES / InChI

Molecular Formula C10H13NO
Molecular Weight 163.2163
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
N-ethylphenyl acetamide (EPA) inhibits DNA synthesis and N-acetylation of 2-aminofluorene in human colon tumor cells (colo 205).
2004 May-Jun
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:00:50 GMT 2023
Edited
by admin
on Sat Dec 16 10:00:50 GMT 2023
Record UNII
J95WO7W7D4
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-PHENYLBUTYRAMIDE
Systematic Name English
.ALPHA.-PHENYLBUTYRAMIDE [MI]
Common Name English
PRIMIDONE IMPURITY C [EP IMPURITY]
Common Name English
2-PHENYLBUTANAMIDE
Systematic Name English
.ALPHA.-ETHYL-.ALPHA.-PHENYLACETAMIDE
Systematic Name English
.ALPHA.-PHENYL-.ALPHA.-ETHYLACETAMIDE
Systematic Name English
BENZENEACETAMIDE, .ALPHA.-ETHYL-
Systematic Name English
PRIMIDONE RELATED COMPOUND C [USP-RS]
Common Name English
EUSTEROL
Common Name English
PRIMIDONE RELATED COMPOUND C
USP-RS  
Common Name English
.ALPHA.-PHENYLBUTYRAMIDE
MI  
Systematic Name English
BUTYRAMIDE, 2-PHENYL-
Systematic Name English
NSC-1861
Code English
PRIMIDONE RELATED COMPOUND C [USP IMPURITY]
Common Name English
Code System Code Type Description
RS_ITEM_NUM
1562033
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
NSC
1861
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
FDA UNII
J95WO7W7D4
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
MERCK INDEX
m886
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY Merck Index
EPA CompTox
DTXSID60870423
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
ECHA (EC/EINECS)
201-980-4
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
CAS
90-26-6
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
PUBCHEM
7011
Created by admin on Sat Dec 16 10:00:51 GMT 2023 , Edited by admin on Sat Dec 16 10:00:51 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
USP
Related Record Type Details
ACTIVE MOIETY