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

Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO
Molecular Weight 121.1366
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FORMANILIDE

SMILES

O=CNC1=CC=CC=C1

InChI

InChIKey=DYDNPESBYVVLBO-UHFFFAOYSA-N
InChI=1S/C7H7NO/c9-6-8-7-4-2-1-3-5-7/h1-6H,(H,8,9)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Methyl analogues of the experimental Alzheimer drug phenserine: synthesis and structure/activity relationships for acetyl- and butyrylcholinesterase inhibitory action.
2001 Nov 22
Synthesis, biological activity, and molecular modeling investigation of new pyrazolo[4,3-e]-1,2,4-triazolo[1,5-c]pyrimidine derivatives as human A(3) adenosine receptor antagonists.
2002 Feb 14
ZEKE photoelectron spectroscopy of the cis and trans isomers of formanilide.
2002 Jan 4
2,9-disubstituted-N6-(arylcarbamoyl)-8-azaadenines as new selective A3 adenosine receptor antagonists: synthesis, biochemical and molecular modelling studies.
2005 Aug 1
Prediction of genotoxicity of chemical compounds by statistical learning methods.
2005 Jun
Direct calculation of electron transfer parameters through constrained density functional theory.
2006 Jul 27
Laser probes of conformational isomerization in flexible molecules and complexes.
2006 Mar 30
Solvent effects on the structural and formyl substrate reactivity properties of a nitrogen/sulfur-ligated zinc hydroxide complex.
2006 May 15
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: A complete structure-activity profile.
2007 Jun
Hexavalent chromium removal from wastewater using aniline formaldehyde condensate coated silica gel.
2007 May 8
Pyrazolo-triazolo-pyrimidines as adenosine receptor antagonists: Effect of the N-5 bond type on the affinity and selectivity at the four adenosine receptor subtypes.
2008 Mar
Synthesis of cationic beta-cyclodextrin derivatives and their applications as chiral stationary phases for high-performance liquid chromatography and supercritical fluid chromatography.
2008 Sep 5
N-Phenyl-formamide.
2009 Jun 20
Hybrid cross-linked polyaniline-WO3 nanocomposite thin film for NO(x) gas sensing.
2009 Mar
3-(1-Naphth-yl)-N-phenyl-oxirane-2-carboxamide.
2009 Nov 21
c-3,t-3-Dimethyl-4-oxo-r-2,c-6-diphenyl-piperidine-1-carboxamide.
2009 Oct 23
Patents
Name Type Language
FORMANILIDE
MI  
Systematic Name English
FORMYLANILINE
Systematic Name English
N-PHENYLFORMAMIDE [HSDB]
Common Name English
FORMANILIDE [MI]
Common Name English
NSC-8862
Code English
N-PHENYLFORMAMIDE
HSDB  
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID3025338
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
CHEBI
42416
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
MESH
C045976
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
CAS
103-70-8
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
NSC
8862
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
HSDB
5355
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
WIKIPEDIA
Formanilide
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
FDA UNII
2805XEA9CL
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
PUBCHEM
7671
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY
MERCK INDEX
m5536
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY Merck Index
ECHA (EC/EINECS)
203-136-0
Created by admin on Fri Dec 15 19:13:04 GMT 2023 , Edited by admin on Fri Dec 15 19:13:04 GMT 2023
PRIMARY