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

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

Approval Year

PubMed

PubMed

TitleDatePubMed
An enzyme-labile safety catch linker for synthesis on a soluble polymeric support.
2001 Mar 2
Novel, potent phenethylamide inhibitors of the hepatitis C virus (HCV) NS3 protease: probing the role of P2 aryloxyprolines with hybrid structures.
2003 Aug 18
The scent of age.
2003 May 7
Thyroid receptor ligands. Part 2: Thyromimetics with improved selectivity for the thyroid hormone receptor beta.
2004 Jul 5
Mandelamide hydrolase from Pseudomonas putida: characterization of a new member of the amidase signature family.
2004 Jun 22
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
SAR and pharmacokinetic studies on phenethylamide inhibitors of the hepatitis C virus NS3/NS4A serine protease.
2004 Sep 6
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
QSAR and pharmacophore analysis on amides against drug-resistant S. aureus.
2008 Jan-Mar
The influence of leukotriene receptors' antagonists on experimentally induced ulcer in rats.
2008 Jul-Sep
Phenylethylamide and phenylmethylamide derivatives as new tyrosinase inhibitors.
2009 Feb
N-(3,4-Diethoxy-phen-yl)acetamide.
2009 May 20
Patents
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