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Details

Stereochemistry ACHIRAL
Molecular Formula C13H11NO
Molecular Weight 197.2325
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BENZANILIDE

SMILES

O=C(NC1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=ZVSKZLHKADLHSD-UHFFFAOYSA-N
InChI=1S/C13H11NO/c15-13(11-7-3-1-4-8-11)14-12-9-5-2-6-10-12/h1-10H,(H,14,15)

HIDE SMILES / InChI

Molecular Formula C13H11NO
Molecular Weight 197.2325
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Design and preparation of sterol mimetics as potential antiparasitics.
2010-10-15
Exploring the effects of H-bonding in synthetic analogues of nickel superoxide dismutase (Ni-SOD): experimental and theoretical implications for protection of the Ni-SCys bond.
2010-08-02
N-(4-Ferrocenylphenyl)benzamide.
2010-06-23
Enantioseparation of benzazoles and benzanilides on polysaccharide-based chiral columns.
2010-05-05
4-Chloro-N-(3,4-dimethyl-phen-yl)benzamide.
2010-04-28
N-(2,4-Dimethyl-phen-yl)-4-methyl-benzamide.
2010-04-21
N-(3-Chloro-phen-yl)-3-methyl-benzamide hemihydrate.
2010-03-31
N-(2,6-Dimethyl-phen-yl)-3-methyl-benzamide.
2010-03-31
2-Methyl-N-p-tolyl-benzamide: a second monoclinic polymorph.
2010-03-24
N-(2-Chloro-phen-yl)-3-methyl-benzamide.
2010-03-20
Fragment-based discovery of selective inhibitors of the Mycobacterium tuberculosis protein tyrosine phosphatase PtpA.
2009-12-15
[External stimulus-responsive conformational alterations of aromatic amides].
2009-12
N-Cyclo-hexyl-3,4,5-trimethoxy-benzamide.
2009-11-28
N-(4-Chloro-phen-yl)-3-methyl-benzamide.
2009-10-17
N-(3,4-Dimethyl-phen-yl)-4-methyl-benzamide.
2009-10-17
N-(2,6-Dichloro-phen-yl)-3-methyl-benzamide.
2009-10-10
Unusual spectral shifts on fast violet-B and benzanilide: Effect of solvents, pH and beta-cyclodextin.
2009-10-01
Pharmacokinetics and tissue distribution of dodeca-2E,4E,8E,10E/Z-tetraenoic acid isobutylamides after oral administration in rats.
2009-10
4-Chloro-N-(3-chloro-phen-yl)benzamide.
2009-09-12
N-(4-Nitro-phen-yl)cinnamamide.
2009-08-08
N-(4-Methoxy-phen-yl)pivalamide.
2009-08-08
N-Benzoyl-N'-(2-chloro-3-pyrid-yl)thio-urea.
2009-07-18
4-Chloro-N-(2,6-dichloro-phen-yl)benzamide.
2009-06-20
4-Chloro-N-cyclo-hexyl-benzamide.
2009-06-10
4-Chloro-N-m-tolyl-benzamide.
2009-05-20
N-(3,4-Diethoxy-phen-yl)acetamide.
2009-05-20
2-Fluoro-N-(4-methoxy-phen-yl)benzamide.
2009-03-19
Determination of a benzamide histone deacetylase inhibitor, MS-275, in human plasma by liquid chromatography with mass-spectrometric detection.
2009-01-15
N-Butyl-4-chloro-benzamide.
2008-11-13
4-Chloro-N-(2-chloro-phen-yl)benzamide.
2008-09-13
Mechanism based QSAR studies of N-phenylbenzamides as antimicrobial agents.
2008-09
N-(4-Chloro-phen-yl)-3,4,5-trimethoxy-benzamide.
2008-07-31
4-Chloro-N-(2,6-dimethyl-phen-yl)benzamide.
2008-06-28
Benzanilides with spasmolytic activity: chemistry, pharmacology, and SAR.
2008-06-01
N-(2,4-Dichloro-phen-yl)benzamide.
2008-05-03
Synthesis and biological evaluation of thiobenzanilides as anticancer agents.
2008-05-01
2,4-Dichloro-N-cyclo-hexyl-benzamide.
2008-04-02
New amido derivatives as potential BKCa potassium channel activators. XI.
2008-04
N-(4-Chloro-phen-yl)benzamide.
2008-03-29
N-(2-Chloro-4-nitro-phen-yl)-2-nitro-benzamide.
2008-03-12
N-(2-Methoxy-phen-yl)-2-nitro-benzamide.
2008-02-20
N-(2,6-Dichloro-phen-yl)benzamide.
2008-01-30
N-(2-Methyl-phen-yl)-2-nitro-benzamide.
2008-01-25
N-(3-Chloro-phen-yl)benzamide.
2008-01-16
Synthesis of 2-arylbenzoxazoles by copper-catalyzed intramolecular oxidative C-O coupling of benzanilides.
2008
Inhibitors of type III secretion in Yersinia: design, synthesis and multivariate QSAR of 2-arylsulfonylamino-benzanilides.
2007-11-15
Structural modifications of benzanilide derivatives, effective potassium channel openers. X.
2006-12
Heterocyclic analogs of benzanilide derivatives as potassium channel activators. IX.
2006-06
Dual fluorescence of diphenyl carbazide and benzanilide: effect of solvents and pH on electronic spectra.
2005-12
Neutron vibrational spectroscopy gives new insights into the structure of poly(p-phenylene terephthalamide).
2005-05-11
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:21:09 GMT 2025
Edited
by admin
on Mon Mar 31 21:21:09 GMT 2025
Record UNII
AK1B12366O
Record Status Validated (UNII)
Record Version
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Name Type Language
BENZANILIDE
MI  
Systematic Name English
NSC-3131
Preferred Name English
N-BENZOYLANILINE
Systematic Name English
BENZANILIDE [MI]
Common Name English
N-PHENYLBENZENECARBOXAMIDE
Systematic Name English
N-PHENYLBENZAMIDE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
202-292-7
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
CAS
93-98-1
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
EPA CompTox
DTXSID9059096
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
PUBCHEM
7168
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
MESH
C034595
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
WIKIPEDIA
BENZANILIDE
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
MERCK INDEX
m2333
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY Merck Index
FDA UNII
AK1B12366O
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY
NSC
3131
Created by admin on Mon Mar 31 21:21:09 GMT 2025 , Edited by admin on Mon Mar 31 21:21:09 GMT 2025
PRIMARY