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ChemicalBook--->CAS DataBase List--->27834-99-7

27834-99-7

27834-99-7 Structure

27834-99-7 Structure
IdentificationMore
[Name]

3-(3-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
[CAS]

27834-99-7
[Synonyms]

ZINC02575227
559253_ALDRICH
Ethyl m-anisoylacetate
Ethyl (m-Methoxybenzoyl)acetate
ETHYL (3-METHOXYBENZOYL)ACETATE
m-Anisoyl-acetic acid ethyl ester
ETHYL 3-(3-METHOXYPHENYL)-3-OXOPROPANOATE
Ethyl 3-(3-Methoxyphenyl)-3-oxopropionate
3-keto-3-(3-methoxyphenyl)propionic acid ethyl ester
Benzenepropanoic acid, 3-methoxy-β-oxo-, ethyl ester
3-(3-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER
[Molecular Formula]

C12H14O4
[MDL Number]

MFCD00086704
[Molecular Weight]

222.24
[MOL File]

27834-99-7.mol
Chemical PropertiesBack Directory
[Boiling point ]

>268 °C(lit.)
[density ]

1.146 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.5360(lit.)
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[form ]

clear liquid
[pka]

10.28±0.46(Predicted)
[color ]

Colorless to Light yellow to Light orange
[CAS DataBase Reference]

27834-99-7(CAS DataBase Reference)
Safety DataBack Directory
[WGK Germany ]

3
[HS Code ]

2918.99.4700
Hazard InformationBack Directory
[Uses]

Reactant involved in:
  • Stereoselective ketonization-olefination of indoles
  • Lewis base catalyzed hydrosilylation and sequential reactions
  • Asymmetric hydrogenation
  • Organocatalytic reduction by trichlorosilane
[Uses]

Reactant involved in:• ;Stereoselective ketonization-olefination of indoles1• ;Lewis base catalyzed hydrosilylation2 and sequential reactions3,4• ;Asymmetric hydrogenation5• ;Organocatalytic reduction by trichlorosilane6
Spectrum DetailBack Directory
[Spectrum Detail]

3-(3-METHOXY-PHENYL)-3-OXO-PROPIONIC ACID ETHYL ESTER(27834-99-7)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

27834-99-7(sigmaaldrich)
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