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Details

Stereochemistry RACEMIC
Molecular Formula C7H12O3
Molecular Weight 144.1684
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL 2-METHYLACETOACETATE

SMILES

CCOC(=O)C(C)C(C)=O

InChI

InChIKey=FNENWZWNOPCZGK-UHFFFAOYSA-N
InChI=1S/C7H12O3/c1-4-10-7(9)5(2)6(3)8/h5H,4H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C7H12O3
Molecular Weight 144.1684
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Enhancement effect of ethyl-2-methyl acetoacetate on triacylglycerols production by a freshwater microalga, Scenedesmus sp. LX1.
2010-12
Environmentally benign periphyton bioreactors for controlling cyanobacterial growth.
2010-12
3,4-Dimethyl-1H-1,2,4-triazepino[2,3-a]benzimidazol-2(3H)-one.
2010-04-17
Effects of a novel allelochemical ethyl 2-methyl acetoacetate (EMA) on the ultrastructure and pigment composition of cyanobacterium Microcystis aeruginosa.
2009-10
Responses of enzymatic antioxidants and non-enzymatic antioxidants in the cyanobacterium Microcystis aeruginosa to the allelochemical ethyl 2-methyl acetoacetate (EMA) isolated from reed (Phragmites communis).
2008-08-25
[Effects of allelochemical EMA from reed on the production and release of cyanotoxins in Microcystis aeruginosa].
2007-09
High production of (2s,3s)-3-hydroxy-2-methylbutanoate by immobilized plant cells of Marchantia polymorpha.
2007-06
Stereochemical consequences of threefold symmetry in asymmetric catalysis: distorting C3 Chiral 1,1,1-tris(oxazolinyl)ethanes ("trisox") in CuII Lewis acid catalysts.
2007
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:30:10 GMT 2025
Edited
by admin
on Mon Mar 31 23:30:10 GMT 2025
Record UNII
NE9WOZ20JE
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYL 2-METHYLACETOACETATE
Systematic Name English
NSC-1102
Preferred Name English
BUTANOIC ACID, 2-METHYL-3-OXO-, ETHYL ESTER
Systematic Name English
2-METHYL-3-OXOBUTYRIC ACID ETHYL ESTER
Systematic Name English
ETHYL 2-ACETYLPROPANOATE
Systematic Name English
ACETOACETIC ACID, .ALPHA.-METHYL-, ETHYL ESTER
Systematic Name English
ETHYL .ALPHA.-METHYLACETOACETATE
Systematic Name English
ETHYL 2-METHYL-3-OXOBUTANOATE
Systematic Name English
ETHYL 3-OXO-2-METHYLBUTANOATE
Systematic Name English
ETHYL .ALPHA.-ACETYLPROPIONATE
Systematic Name English
.ALPHA.-METHYLACETOACETIC ESTER
Systematic Name English
ACETOACETIC ACID, 2-METHYL-, ETHYL ESTER
Systematic Name English
ETHYL .ALPHA.-METHYLACETYLACETATE
Systematic Name English
ETHYL (±)-2-METHYLACETOACETATE
Systematic Name English
2-METHYL-3-OXOBUTANOIC ACID ETHYL ESTER
Systematic Name English
ETHYL 2-METHYL-3-OXOBUTYRATE
Systematic Name English
2-METHYLACETOACETIC ACID ETHYL ESTER
Systematic Name English
ETHYL 2-ACETYLPROPIONATE
Systematic Name English
ETHYL METHYLACETOACETATE
Systematic Name English
Code System Code Type Description
ECHA (EC/EINECS)
210-179-9
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
PRIMARY
NSC
1102
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
PRIMARY
PUBCHEM
701
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
PRIMARY
EPA CompTox
DTXSID2033493
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
PRIMARY
FDA UNII
NE9WOZ20JE
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
PRIMARY
CAS
609-14-3
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
PRIMARY
CAS
1522-45-8
Created by admin on Mon Mar 31 23:30:10 GMT 2025 , Edited by admin on Mon Mar 31 23:30:10 GMT 2025
ALTERNATIVE