Ethyl oxophenylacetate

Modify Date: 2024-01-02 14:10:24

Ethyl oxophenylacetate Structure
Ethyl oxophenylacetate structure
Common Name Ethyl oxophenylacetate
CAS Number 1603-79-8 Molecular Weight 178.185
Density 1.1±0.1 g/cm3 Boiling Point 256.5±0.0 °C at 760 mmHg
Molecular Formula C10H10O3 Melting Point 97ºC
MSDS Chinese USA Flash Point 111.4±15.9 °C

 Use of Ethyl oxophenylacetate


Ethyl phenylglyoxylate (Ethyl benzoylformate; Phenylglyoxylic acid ethyl ester) is the ethyl ester of phenylglyoxylic acid, used as a synthetic reagent[1].

 Names

Name ethyl phenylglyoxylate
Synonym More Synonyms

 Ethyl oxophenylacetate Biological Activity

Description Ethyl phenylglyoxylate (Ethyl benzoylformate; Phenylglyoxylic acid ethyl ester) is the ethyl ester of phenylglyoxylic acid, used as a synthetic reagent[1].
Related Catalog
References

[1]. Shengkui Hu, et al. Photochemically Active Polymers Containing Pendant Ethyl Phenylglyoxylate. Macromolecules 1998, 31, 2, 322–327.

 Chemical & Physical Properties

Density 1.1±0.1 g/cm3
Boiling Point 256.5±0.0 °C at 760 mmHg
Melting Point 97ºC
Molecular Formula C10H10O3
Molecular Weight 178.185
Flash Point 111.4±15.9 °C
Exact Mass 178.062988
PSA 43.37000
LogP 1.80
Vapour Pressure 0.0±0.5 mmHg at 25°C
Index of Refraction 1.513

 Safety Information

Personal Protective Equipment Eyeshields;Gloves
Hazard Codes Xi: Irritant;
Safety Phrases S24/25
RIDADR NONH for all modes of transport
HS Code 2942000000

 Synthetic Route

 Customs

HS Code 2918300090
Summary 2918300090 other carboxylic acids with aldehyde or ketone function but without other oxygen function, their anhydrides, halides, peroxides, peroxyacids and their derivatives。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:6.5%。General tariff:30.0%

 Articles2

More Articles
98% Enantioselectivity in the asymmetric synthesis of a useful chiral building block by heterogeneous method: Enantioselective hydrogenation of ethyl-benzoylformate over cinchona modified Pt/Al2 O3 catalysts in the acetic acid. Sutyinszki M, et al.

Catal. Commun. 3(3) , 125-7, (2002)

Preparation of chiral 5-deazaflavin derivatives and their asymmetric reduction of ethyl benzoylformate. Tanaka K, et al.

Tetrahedron Lett. 25(16) , 1741-2, (1984)

 Synonyms

ethyl 2-oxo-2-phenylacetate
Ethyl phenylglyoxylate
Ethyl oxophenylacetate
Glyoxylic acid, phenyl-, ethyl ester (8CI)
Ethyloxo(phenyl)acetat
Benzoylformic Acid Ethyl Ester
Phenylglyoxylic Acid Ethyl Ester
Ethyl oxo(phenyl)acetate
ethyl phenyloxoacetate
Glyoxylic acid, phenyl-, ethyl ester
MFCD00009120
ETHYL α-OXOBENZENEACETATE
EINECS 216-504-0
Benzeneacetic acid, α-oxo-, ethyl ester
Ethyl benzoylformate
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