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Details

Stereochemistry ACHIRAL
Molecular Formula C8H9NO
Molecular Weight 135.1632
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZENEACETAMIDE

SMILES

NC(=O)CC1=CC=CC=C1

InChI

InChIKey=LSBDFXRDZJMBSC-UHFFFAOYSA-N
InChI=1S/C8H9NO/c9-8(10)6-7-4-2-1-3-5-7/h1-5H,6H2,(H2,9,10)

HIDE SMILES / InChI

Molecular Formula C8H9NO
Molecular Weight 135.1632
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Synthesis and structure-activity relationships of N-(1-benzylpiperidin-4-yl)arylacetamide analogues as potent sigma1 receptor ligands.
2001 Dec 6
Role of alphaArg145 and betaArg263 in the active site of penicillin acylase of Escherichia coli.
2002 Jul 1
Synthesis and antimicrobial activity of some novel 2-(p-substituted-phenyl)-5-substituted-carbonylaminobenzoxazoles.
2002 Mar
Novel, potent phenethylamide inhibitors of the hepatitis C virus (HCV) NS3 protease: probing the role of P2 aryloxyprolines with hybrid structures.
2003 Aug 18
Bhimamycin A to approximately E and bhimanone: isolation, structure elucidation and biological activity of novel quinone antibiotics from a terrestrial Streptomycete.
2003 Nov
Studies on the metabolism of the novel, selective cyclooxygenase-2 inhibitor indomethacin phenethylamide in rat, mouse, and human liver microsomes: identification of active metabolites.
2004 Jan
Design, synthesis, and biological evaluation of new 8-heterocyclic xanthine derivatives as highly potent and selective human A2B adenosine receptor antagonists.
2004 Mar 11
Studies on anti-Helicobacter pylori agents. Part 3: A novel, efficacious cephem derivative, FR193879.
2004 May 17
Synthesis and receptor binding studies of 3-substituted piperazine derivatives.
2006 Mar
Diastereospecific photocyclization of a isopropylbenzophenone derivative in crystals and the morphological changes.
2007 Aug 31
Production of enantiomerically pure (S)-beta-phenylalanine and (R)-beta-phenylalanine by penicillin G acylase from Escherichia coli in aqueous medium.
2007 Dec
2,2-Dichloro-N-(2,3-dimethyl-phen-yl)acetamide.
2007 Dec 12
The influence of leukotriene receptors' antagonists on experimentally induced ulcer in rats.
2008 Jul-Sep
Regulation of phenylacetic acid degradation genes of Burkholderia cenocepacia K56-2.
2009 Oct 18
2,3-Disubstituted acrylamides as potent glucokinase activators.
2010 Oct 1
Structural characterization of the Hepatitis C Virus NS3 protease from genotype 3a: the basis of the genotype 1b vs. 3a inhibitor potency shift.
2010 Sep 30
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:18:58 GMT 2023
Edited
by admin
on Sat Dec 16 04:18:58 GMT 2023
Record UNII
5R219M9TJF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BENZENEACETAMIDE
Systematic Name English
PHENACETAMIDE
Common Name English
PHENYL-.BETA.-ACETYLAMINE
Common Name English
PHENYLACETAMIDE
Common Name English
PHENYLACETIC ACID AMIDE
Systematic Name English
BENZENEDIACETAMIDE
Systematic Name English
.ALPHA.-TOLUAMIDE
Systematic Name English
NSC-1877
Code English
.ALPHA.-TOLUIMIDIC ACID
Systematic Name English
ACETAMIDE, 2-PHENYL-
Systematic Name English
.ALPHA.-PHENYLACETAMIDE [MI]
Common Name English
2-PHENYLACETAMIDE
Systematic Name English
.ALPHA.-PHENYLACETAMIDE
MI  
Systematic Name English
Code System Code Type Description
CAS
103-81-1
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
EPA CompTox
DTXSID1059282
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
NSC
1877
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
PUBCHEM
7680
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
MESH
C005293
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
MERCK INDEX
m8648
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
203-147-0
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
FDA UNII
5R219M9TJF
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY
CHEBI
16562
Created by admin on Sat Dec 16 04:18:58 GMT 2023 , Edited by admin on Sat Dec 16 04:18:58 GMT 2023
PRIMARY