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

Details

Stereochemistry ACHIRAL
Molecular Formula C6H10O3
Molecular Weight 130.1418
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Ethyl Acetoacetate

SMILES

CCOC(=O)CC(C)=O

InChI

InChIKey=XYIBRDXRRQCHLP-UHFFFAOYSA-N
InChI=1S/C6H10O3/c1-3-9-6(8)4-5(2)7/h3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H10O3
Molecular Weight 130.1418
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
7,7'-Dihy-droxy-4,4'-dimethyl-3,4-dihydro-2H,2'H-4,6'-bichromene-2,2'-dione.
2010-12-18
Synthesis and antimicrobial activity of 1,2,3-triazoles containing quinoline moiety.
2010-12
A short synthesis of the triazolopyrimidine antibiotic essramycin.
2010-11-29
Synthesis, antimicrobial, and mosquito larvicidal activity of 1-aryl-4-methyl-3,6-bis-(5-methylisoxazol-3-yl)-2-thioxo-2,3,6,10b-tetrahydro-1H-pyrimido[5,4-c]quinolin-5-ones.
2010-10-15
Spectroscopic, solvent influence and thermal studies of ternary copper(II) complexes of diester and dinitrogen base ligands.
2010-10-15
Green one pot solvent-free synthesis of pyrano[2,3-c]-pyrazoles and pyrazolo[1,5-a]pyrimidines.
2010-09-20
cBSA-147 for the preparation of bacterial biofilms in a microchannel reactor.
2010-09
Synthesis of novel fluorescent cyclohexenone derivatives and their partitioning study in ionic micellar media.
2010-09
A versatile synthesis of fumaquinone.
2010-08-06
L-Histidine and L-arginine promote Knoevenagel reaction in water.
2010-08
1-Isopropenyl-1H-1,3-benzimidazol-2(3H)-one.
2010-05-22
4-Methyl-2,3-dihydro-1H-1,5-benzodiazepin-2-one monohydrate.
2010-05-22
Bioreduction of some common carbonylic compounds mediated by yeasts.
2010-04-02
Characterization of alcohol dehydrogenase from permeabilized brewer's yeast cells immobilized on the derived attapulgite nanofibers.
2010-04
Ethyl 2-acetyl-3-(4-bromo-anilino)butanoate.
2010-01-09
Superabsorbed alcohol dehydrogenase--a new catalyst for asymmetric reductions.
2009-11
Using a water-immiscible ionic liquid to improve asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one catalyzed by immobilized Candida parapsilosis CCTCC M203011 cells.
2009-10-22
(Z)-Ethyl 3-(2,4,6-trimethyl-anilino)but-2-enoate.
2009-10-17
Ethyl 4-(3-hydroxy-phen-yl)-2,7,7-trimethyl-5-oxo-1,4,5,6,7,8-hexa-hydro-quinoline-3-carboxyl-ate.
2009-10-07
Redetermination of ethyl (3a-cis)-3a,8b-dihydr-oxy-2-methyl-4-oxo-3a,8b-dihydro-4H-indeno[1,2-b]furan-3-carboxyl-ate monohydrate.
2009-10-03
Diethyl 2,6-dimethyl-pyridine-3,5-dicarboxyl-ate at 100 K.
2009-09-26
Synthesis and pharmacological investigation of 3-(substituted 1-phenylethanone)-4-(substituted phenyl)-1, 2, 3, 4-tetrahydropyrimidine-5-carboxylates.
2009-09
9-Eth-oxy-1,5,13-trimethyl-8,10-dioxa-tetra-cyclo-[7.7.1.0.0]hepta-deca-2,4,6,11,13,15-hexa-ene.
2009-08-22
Photoactive diazoketo-functionalized self-assembled monolayer for biomolecular patterning.
2009-08-18
Ethyl 2-acetyl-3-(4-chloro-anilino)butanoate.
2009-08-08
A synthetic coumarin (4-methyl-7 hydroxy coumarin) has anti-cancer potentials against DMBA-induced skin cancer in mice.
2009-07-01
Studies with arylhydrazonopyridinones: Synthesis of new arylhydrazono thieno[3,4-c]pyridinones as novel D2T2 dye class; classical verse green methodologies.
2009-06
Straightforward and highly efficient catalyst-free one-step synthesis of 2-(purin-6-yl)acetoacetic acid ethyl esters, (purin-6-yl)acetates, and 6-methylpurines through S(N)Ar-based reactions of 6-halopurines with ethyl acetoacetate.
2009-04-16
Isolation and crystal structures of both enol and keto tautomer intermediates in a hydration of an alkyne-carboxylic acid ester catalyzed by iridium complexes in water.
2008-12-17
L-Proline as an efficient and reusable promoter for the synthesis of coumarins in ionic liquid.
2008-12
Synthesis of novel 6,6'-methylene-bis-[3-(2-anilinoacetyl)-4-hydroxycoumarin] derivatives.
2008-12
Lead exposure study among workers in lead acid battery repair units of transport service enterprises, Addis Ababa, Ethiopia: a cross-sectional study.
2008-11-28
5-Methyl-1-phenyl-1H-1,2,3-triazole-4-carboxylic acid.
2008-08-30
Novel quinolinonyl diketo acid derivatives as HIV-1 integrase inhibitors: design, synthesis, and biological activities.
2008-08-14
Ethyl 6-methyl-2-oxo-4-phenyl-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate.
2008-08-13
Yeast cell factories for fine chemical and API production.
2008-08-07
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.
2008-07-29
Ethyl 4-(2-bromo-5-fluoro-phen-yl)-6-methyl-1-phenyl-2-thioxo-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate.
2008-07-19
Lewis acid-mediated reactions of 1-cyclopropyl-2-arylethanone derivatives with allenic ester, ethyl acetoacetate, and methyl acrylate.
2008-07-18
P-TSA catalyzed facile and efficient synthesis of polyhydroquinoline derivatives through hantzsch multi-component condensation.
2008-07
The solvent-free synthesis of 1,4-dihydropyridines under ultrasound irradiation without catalyst.
2008-07
Ethyl 6-methyl-4-[2-(4,4,5,5-tetra-methyl-1,3,2-dioxaborolan-2-yl)thio-phen-3-yl]-2-thioxo-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate.
2008-04-26
2-(4-Chloro-benzoyl-meth-yl)-2H-1,4-benzothia-zin-3(4H)-one.
2008-03-29
Synthesis of progesterone heterocyclic derivatives of potential antimicrobial activity.
2008-03
Ethyl 4-(3-bromo-2-thien-yl)-2-oxo-6-phenyl-cyclo-hex-3-ene-1-carboxyl-ate.
2008-02-06
N-(1-Naphth-yl)acetoacetamide.
2008-01-30
Ethyl 6-(2-chloro-phen-yl)-4-methyl-1-(3-oxobut-yl)-2-thioxo-1,2,3,6-tetra-hydro-pyrimidine-5-carboxyl-ate.
2008-01-04
Use of Raman spectroscopy as an in situ tool to obtain kinetic data for organic transformations.
2008
An enantioselective biginelli reaction catalyzed by a simple chiral secondary amine and achiral brønsted acid by a dual-activation route.
2008
Ethyl 4-(4-hydroxy-phen-yl)-6-methyl-2-thioxo-1,2,3,4-tetra-hydro-pyrimidine-5-carboxyl-ate monohydrate.
2007-12-12
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:49:13 GMT 2025
Edited
by admin
on Mon Mar 31 18:49:13 GMT 2025
Record UNII
IZP61H3TB1
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2415
Preferred Name English
Ethyl Acetoacetate
FCC   FHFI   HSDB   INCI   MI  
INCI  
Official Name English
ETHYL 3-OXYBUTANOATE
Common Name English
ETHYL ACETOACETATE [HSDB]
Common Name English
ACETOACETIC ESTER
Common Name English
ETHYL ACETOACETATE [FCC]
Common Name English
NSC-8657
Code English
ETHYL ACETOACETATE [FHFI]
Common Name English
ETHYL 2-METHYL-3-OXOPROPIONATE
Systematic Name English
BUTANOIC ACID, 3-OXO-, ETHYL ESTER
Common Name English
NSC-37390
Code English
NSC-657
Code English
3-OXOBUTANOIC ACID ETHYL ESTER
Systematic Name English
ACETOACETIC ACID, ETHYL ESTER
Common Name English
ETHYL ACETOACETATE [MI]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION ETHYL ACETOACETATE
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
Code System Code Type Description
EVMPD
SUB91402
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
NSC
37390
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
CAS
141-97-9
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
DAILYMED
IZP61H3TB1
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
PUBCHEM
8868
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
CHEBI
4893
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
MERCK INDEX
m5082
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY Merck Index
RXCUI
1603474
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY RxNorm
HSDB
402
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
WIKIPEDIA
ETHYL ACETOACETATE
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
EPA CompTox
DTXSID2027092
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
ECHA (EC/EINECS)
205-516-1
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
FDA UNII
IZP61H3TB1
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
JECFA MONOGRAPH
472
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
MESH
C024840
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
NSC
8657
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
SMS_ID
100000141274
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY
NSC
657
Created by admin on Mon Mar 31 18:49:13 GMT 2025 , Edited by admin on Mon Mar 31 18:49:13 GMT 2025
PRIMARY