CAS 1603-79-8

Etilo benzoilformato

Descripción:

Etilo benzoilformato, con el número CAS 1603-79-8, es un compuesto orgánico que pertenece a la clase de los ésteres. Se caracteriza por su estructura, que incluye un grupo etilo, un moiety de bencilo y un grupo formiato. Este compuesto típicamente aparece como un líquido incoloro a amarillo pálido con un agradable olor aromático. Etilo benzoilformato es conocido por su papel como agente saborizante y fragancia en diversas aplicaciones, incluyendo alimentos y cosméticos. Es soluble en disolventes orgánicos y exhibe una estabilidad moderada en condiciones estándar. El compuesto puede sufrir hidrólisis en presencia de agua, lo que lleva a la formación de ácido benciloformico y etanol. Etilo benzoilformato también es de interés en la química orgánica sintética, donde puede servir como un intermedio en la síntesis de otros compuestos químicos. Al igual que muchas sustancias orgánicas, se deben tomar precauciones de seguridad al manipularlo, ya que puede causar irritación en la piel y los ojos.

Fórmula: C₁₀H₁₀O₃

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

Clave InChI: InChIKey=QKLCQKPAECHXCQ-UHFFFAOYSA-N

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

Sinónimos:

• 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

Fórmula: C₁₀H₁₀O₃

Pureza: >96.0%(GC)

Forma y color: Colorless to Yellow clear liquid

Peso molecular: 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

Fórmula: C₁₀H₁₀O₃

Pureza: 98%

Forma y color: Clear colorless to yellow, Liquid

Peso molecular: 178.19

Ref: 02-B25292

Benzeneacetic acid, α-oxo-, ethyl ester

CAS: 1603-79-8

Fórmula: C₁₀H₁₀O₃

Pureza: 95%

Forma y color: Liquid

Peso molecular: 178.1846

Ref: IN-DA001RUA

Ethyl phenylglyoxylate

CAS: 1603-79-8

Ethyl phenylglyoxylate

Pureza: ≥98%

Peso molecular: 178.18g/mol

Ref: 54-BUP19691

2-Phenyl-2-oxoacetic acid ethyl ester

CAS: 1603-79-8

Fórmula: C₁₀H₁₀O₃

Forma y color: Neat

Peso molecular: 178.18

Ref: 04-C16068500

Ethyl oxo(phenyl)acetate

CAS: 1603-79-8

Ethyl oxo(phenyl)acetate

Fórmula: C₁₀H₁₀O₃

Pureza: 98%

Forma y color: pale yellow liquid

Peso molecular: 178.18g/mol

Ref: 54-OR6395

Ethyl Benzoylformate

CAS: 1603-79-8

Fórmula: C₁₀H₁₀O₃

Peso molecular: 178.19

Ref: 4Z-G-3232

Ethyl Benzoylformate

CAS: 1603-79-8

Fórmula: C₁₀H₁₀O₃

Pureza: 98%

Forma y color: Liquid

Peso molecular: 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.

Fórmula: C₁₀H₁₀O₃

Pureza: 98.46%

Forma y color: Yellow Liquid

Peso molecular: 178.18

Ref: TM-T20351

Ethyl Benzoylformate

Producto controlado

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);

Fórmula: C₁₀H₁₀O₃

Forma y color: Neat

Peso molecular: 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.

Fórmula: C₁₀H₁₀O₃

Pureza: Min. 95%

Peso molecular: 178.18 g/mol

Ref: 3D-FE33198