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Details

Stereochemistry ACHIRAL
Molecular Formula C10H11NO2
Molecular Weight 177.1998
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ACETOACETANILIDE

SMILES

CC(=O)CC(=O)NC1=CC=CC=C1

InChI

InChIKey=DYRDKSSFIWVSNM-UHFFFAOYSA-N
InChI=1S/C10H11NO2/c1-8(12)7-10(13)11-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H,11,13)

HIDE SMILES / InChI

Molecular Formula C10H11NO2
Molecular Weight 177.1998
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Metal-induced cyclization of thiosemicarbazones derived from beta-keto amides and beta-keto esters: open-chain and cyclized ligands in zinc(II) complexes.
2002 Mar 25
Synthesis, characterization, and antifungal studies of transition metal complexes of omega-bromoacetoacetanilide isonicotinylhydrazone.
2004 Jul-Sep
Selective electrochemical sensor for copper (II) ion based on chelating ionophores.
2006 Aug 4
Development of novel reagent for Hantzsch reaction for the determination of formaldehyde by spectrophotometry and fluorometry.
2007 Apr
Knorr cyclizations and distonic superelectrophiles.
2007 Dec 7
Flow-injection spectrofluorometric determination of trace amounts of formaldehyde in water after derivatization with acetoacetanilide.
2007 Jul 31
Spectroscopic, and thermal studies of some new binuclear transition metal(II) complexes with hydrazone ligands containing acetoacetanilide and isoxazole.
2007 Nov
Synthesis, spectral, catalytic and antimicrobial studies of PPh3/AsPh3 complexes of Ru(II) with dibasic tridentate O, N, S donor ligands.
2007 Sep
Simple fluorimetric method for quantification of sialic acids in glycoproteins.
2008 Apr 1
Synthesis and antimicrobial activity of some new pyrazole, fused pyrazolo[3,4-d]-pyrimidine and pyrazolo[4,3-e][1,2,4]-triazolo[1,5-c]pyrimidine derivatives.
2008 Jul 29
Syntheses of 1,3-imidazolin-2-ones and 1,3-imidazolin-2-thiones from new building blocks, gamma-aminoacetoacetanilides.
2008 Nov-Dec
Mononuclear Ru(III) Schiff base complexes: synthesis, spectral, redox, catalytic and biological activity studies.
2009 Apr
N-(3,4-Dichloro-phen-yl)-3-oxo-butanamide.
2009 Dec 4
Formaldehyde in the indoor environment.
2010 Apr 14
Acetoacetanilides as masked isocyanates: facile and efficient synthesis of unsymmetrically substituted ureas.
2010 Oct 1
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:20:45 GMT 2023
Edited
by admin
on Fri Dec 15 17:20:45 GMT 2023
Record UNII
W35JB9PY3X
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ACETOACETANILIDE
HSDB   MI  
Systematic Name English
1-(PHENYLAMINO)-1,3-1-(PHENYLCARBAMOYL)-2-PROPANONE
Common Name English
ACETOACETANILIDE [MI]
Common Name English
ACETOACETANILIDE [HSDB]
Common Name English
.ALPHA.-ACETYLACETANILIDE
Systematic Name English
N-PHENYLACETYLACETAMIDE
Systematic Name English
NSC-2656
Code English
N-(ACETOACETYL)ANILINE
Systematic Name English
ACETOACETAMIDOBENZENE
Systematic Name English
3-OXO-N-PHENYLBUTANAMIDE
Systematic Name English
3-OXO-N-PHENYLBUTYRAMIDE
Systematic Name English
4-(PHENYLAMINO)-2,4-BUTANEDIONE
Systematic Name English
N-PHENYL-3-OXOBUTANAMIDE
Systematic Name English
ACETOACETIC ACID ANILIDE
Common Name English
N-PHENYLACETOACETAMIDE
Systematic Name English
BUTANAMIDE, 3-OXO-N-PHENYL-
Systematic Name English
.ALPHA.-KETOBUTYRANILIDE
Systematic Name English
ACETOACETIC ANILIDE
Common Name English
.ALPHA.-ACETYL-N-PHENYLACETAMIDE
Systematic Name English
1-(PHENYLAMINO)-1,3-BUTANEDIONE
Systematic Name English
Code System Code Type Description
MERCK INDEX
m1327
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY Merck Index
WIKIPEDIA
Acetoacetanilide
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
CAS
102-01-2
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
MESH
C056965
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID0024397
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
NSC
2656
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
FDA UNII
W35JB9PY3X
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-996-4
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
HSDB
2669
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY
PUBCHEM
7592
Created by admin on Fri Dec 15 17:20:45 GMT 2023 , Edited by admin on Fri Dec 15 17:20:45 GMT 2023
PRIMARY