CAS 1603-79-8

Etil benzoilformato

Descrizione:

Etil benzoilformato, con il numero CAS 1603-79-8, è un composto organico che appartiene alla classe degli esteri. È caratterizzato dalla sua struttura, che include un gruppo etile, un gruppo benzilico e un gruppo formiato. Questo composto appare tipicamente come un liquido incolore o giallo pallido con un piacevole odore aromatico. Etil benzoilformato è noto per il suo ruolo come agente aromatizzante e fragranza in varie applicazioni, tra cui alimenti e cosmetici. È solubile in solventi organici e presenta una stabilità moderata in condizioni standard. Il composto può subire idrolisi in presenza di acqua, portando alla formazione di acido benzilformico ed etanolo. Etil benzoilformato è anche di interesse nella chimica organica sintetica, dove può fungere da intermediario nella sintesi di altri composti chimici. Come molte sostanze organiche, è necessario adottare precauzioni di sicurezza quando lo si maneggia, poiché può causare irritazione alla pelle e agli occhi.

Formula: C₁₀H₁₀O₃

InChI: InChI=1S/C10H10O3/c1-2-13-10(12)9(11)8-6-4-3-5-7-8/h3-7H,2H2,1H3

InChI key: InChIKey=QKLCQKPAECHXCQ-UHFFFAOYSA-N

SMILES: C(C(OCC)=O)(=O)C1=CC=CC=C1

Sinonimi:

• 2-Oxo-2-phenylacetic acid ethyl ester
• 2-Phenyl-2-oxoacetic acid ethyl ester
• Benzeneacetic acid, α-oxo-, ethyl ester
• Benzoylformic acid ethyl ester
• Ethyl 2-oxo-2-phenylacetate
• Ethyl 2-phenyl-2-oxoacetate
• Ethyl Oxo(Phenyl)Acetate
• Ethyl benzoyl formate
• Ethyl oxophenylacetate
• Ethyl phenylglyoxylate
• Ethyl α-oxobenzeneacetate
• Ethylphenylglyoxylate
• Glyoxylic acid, phenyl-, ethyl ester
• NSC 6766
• Phenylglyoxylic acid ethyl ester
• α-Oxobenzeneacetic acid ethyl ester

Ethyl Benzoylformate

CAS: 1603-79-8

Formula: C₁₀H₁₀O₃

Purezza: >96.0%(GC)

Colore e forma: Colorless to Yellow clear liquid

Peso molecolare: 178.19

Ref: 3B-B0109

Ethyl phenylglyoxylate, 98%

CAS: 1603-79-8

Ethyl phenylglyoxylate has been used in preparation of 1,5-dihydro-5-deazaflavin derivatives possessing a chiral substituent at N(3) position. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to

Formula: C₁₀H₁₀O₃

Purezza: 98%

Colore e forma: Clear colorless to yellow, Liquid

Peso molecolare: 178.19

Ref: 02-B25292

Benzeneacetic acid, α-oxo-, ethyl ester

CAS: 1603-79-8

Formula: C₁₀H₁₀O₃

Purezza: 95%

Colore e forma: Liquid

Peso molecolare: 178.1846

Ref: IN-DA001RUA

Ethyl phenylglyoxylate

CAS: 1603-79-8

Ethyl phenylglyoxylate

Purezza: ≥98%

Peso molecolare: 178.18g/mol

Ref: 54-BUP19691

2-Phenyl-2-oxoacetic acid ethyl ester

CAS: 1603-79-8

Formula: C₁₀H₁₀O₃

Colore e forma: Neat

Peso molecolare: 178.18

Ref: 04-C16068500

Ethyl oxo(phenyl)acetate

CAS: 1603-79-8

Ethyl oxo(phenyl)acetate

Formula: C₁₀H₁₀O₃

Purezza: 98%

Colore e forma: pale yellow liquid

Peso molecolare: 178.18g/mol

Ref: 54-OR6395

Ethyl Benzoylformate

CAS: 1603-79-8

Formula: C₁₀H₁₀O₃

Peso molecolare: 178.19

Ref: 4Z-G-3232

Ethyl Benzoylformate

CAS: 1603-79-8

Formula: C₁₀H₁₀O₃

Purezza: 98%

Colore e forma: Liquid

Peso molecolare: 178.187

Ref: 10-F035199

Ethyl phenylglyoxylate

CAS: 1603-79-8

Ethyl phenylglyoxylate (AI3 10033) is a simultaneous inhibitor and substrate of chicken liver carboxylesterase.

Formula: C₁₀H₁₀O₃

Purezza: 98.46%

Colore e forma: Yellow Liquid

Peso molecolare: 178.18

Ref: TM-T20351

Ethyl Benzoylformate

Prodotto controllato

CAS: 1603-79-8

Applications Ethyl Benzoylformate is a general chemical reagent used in the preparation of diaminoethanediyl bismethylpyridinium salts for designing recyclable organocatalysts.
References Lisnyak, V. et al.: J. Org. Chem., 80, 8570 (2015);

Formula: C₁₀H₁₀O₃

Colore e forma: Neat

Peso molecolare: 178.18

Ref: TR-E899995

Ethyl benzoylformate

CAS: 1603-79-8

Ethyl benzoylformate is a chemical compound that belongs to the group of cinchona alkaloids. It is used as an analytical reagent for determining the concentration of cinchonidine, which assists in the diagnosis and treatment of inflammatory diseases. The biosynthesis of ethyl benzoylformate begins with the condensation reaction between fatty acid and dinucleotide phosphate. This reaction can be enhanced by adding a cationic surfactant to increase the rate at which it takes place. The redox potentials of this compound are important in understanding its reactivity because they indicate whether it will oxidize or reduce another molecule. Ethyl benzoylformate has been shown to act as an adrenergic receptor agonist in lutea l., a model system for studying adrenergic receptors. Its asymmetric synthesis is achieved through two different routes, one requiring ethyl formate and one not requiring it.

Formula: C₁₀H₁₀O₃

Purezza: Min. 95%

Peso molecolare: 178.18 g/mol

Ref: 3D-FE33198