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3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER

CAS No.
51725-82-7
Chemical Name:
3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER
Synonyms
Ethyl o-toluoylacetate;3-OXO-3-O-TOLYLPROPANOATE;Ethyl o-methylbenzoylacetate;ETHYL (2-METHYLBENZOYL)ACETATE;ETHYL 3-OXO-3-O-TOLYLPROPANOATE;Ethyl 2-(2-methylbenzoyl)acetate;Ethyl 3-Oxo-3-(o-tolyl)propionate;Ethyl (2-methylbenzoyl)acetate 97%;2-Methylbenzoylacetic acid ethyl ester;2-[(2-methylphenyl)-oxomethyl]butanoate
CBNumber:
CB7747245
Molecular Formula:
C12H14O3
Molecular Weight:
206.24
MDL Number:
MFCD03424817
MOL File:
51725-82-7.mol
MSDS File:
SDS
Last updated:2023-06-08 17:06:38

3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER Properties

Boiling point 256-257 °C(lit.)
Density 1.069 g/mL at 25 °C(lit.)
refractive index n20/D 1.5255(lit.)
Flash point >230 °F
storage temp. Sealed in dry,Room Temperature
pka 10.00±0.46(Predicted)
form clear liquid
color Colorless to Light yellow to Light orange
λmax 287nm(MeOH)(lit.)
CAS DataBase Reference 51725-82-7(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

WGK Germany  3
HS Code  2918.30.3000
NFPA 704
1
0 0

3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TCI Chemical E1125 Ethyl (2-Methylbenzoyl)acetate >98.0%(T) 51725-82-7 1g $116 2024-03-01 Buy
TRC E572630 ethyl3-(2-methylphenyl)-3-oxopropanoate 51725-82-7 50mg $65 2021-12-16 Buy
TRC E572630 ethyl3-(2-methylphenyl)-3-oxopropanoate 51725-82-7 10mg $45 2021-12-16 Buy
AK Scientific 7228AB Ethyl2-(2-methylbenzoyl)acetate 51725-82-7 1g $54 2021-12-16 Buy
AK Scientific J99197 Ethyl2-(2-methylbenzoyl)acetate 51725-82-7 1g $40 2021-12-16 Buy
Product number Packaging Price Buy
E1125 1g $116 Buy
E572630 50mg $65 Buy
E572630 10mg $45 Buy
7228AB 1g $54 Buy
J99197 1g $40 Buy

3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER Chemical Properties,Uses,Production

Uses

Reactant for:• ;Preparation of highly substituted furans by tandem condensation-cyclization reactions using bismuth triflate catalyst1• ;Co/Mn-mediated oxidative cross-coupling2• ;Enantioselective ruthenium-catalyzed hydrogenation3• ;Preparation of cambinol analogs for sirtuin inhibition with antitumor action4

Uses

Reactant for:

  • Preparation of highly substituted furans by tandem condensation-cyclization reactions using bismuth triflate catalyst
  • Co/Mn-mediated oxidative cross-coupling
  • Enantioselective ruthenium-catalyzed hydrogenation
  • Preparation of cambinol analogs for sirtuin inhibition with antitumor action

General Description

Ethyl (2-methylbenzoyl)acetate is a β-keto ester. It undergoes Co/Mn mediated oxidative coupling reaction with various indole derivatives.

118-90-1
51725-82-7
Synthesis of 3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER from o-Toluic acid
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View Lastest Price from 3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER pictures 2019-12-23 3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER
51725-82-7
US $1.00 / KG 1KG 99% 100KG Career Henan Chemical Co

3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER Spectrum

3-OXO-3-O-TOLYLPROPANOATE Ethyl 2-(2-methylbenzoyl)acetate Ethyl o-methylbenzoylacetate Ethyl o-toluoylacetate Ethyl (2-methylbenzoyl)acetate 97% ETHYL (2-METHYLBENZOYL)ACETATE ETHYL 3-OXO-3-O-TOLYLPROPANOATE 3-OXO-3-O-TOLYL-PROPIONIC ACID ETHYL ESTER 3-OXO-3-(2-TOLYL)PROPIONIC ACID ETHYL ESTER 2-Methylbenzoylacetic acid ethyl ester 3-(2-Methylphenyl)-3-oxopropionic acid ethyl ester 3-Oxo-3-(2-methylphenyl)propanoic acid ethyl ester 3-Oxo-3-(2-methylphenyl)propionic acid ethyl ester β-Oxo-2-methylbenzenepropionic acid ethyl ester 2-[(2-methylphenyl)-oxomethyl]butanoate Benzenepropanoic acid, 2-methyl-β-oxo-, ethyl ester Ethyl 3-Oxo-3-(o-tolyl)propionate Benzenepropanoicacid,2-methyl-β-oxo-,ethylester 51725-82-7 Esters Organic Building Blocks Building Blocks Carbonyl Compounds C12 to C63 Building Blocks C12 to C63 Carbonyl Compounds Chemical Synthesis Organic Building Blocks C12 to C63 Carbonyl Compounds Esters