CAS 90315-82-5

Etil (R)-2-hidroxi-4-fenilbutirato

Descripción:

Etil (R)-2-hidroxi-4-fenilbutirato, con el número CAS 90315-82-5, es un compuesto orgánico caracterizado por su grupo funcional éster, que se deriva de la reacción de un ácido carboxílico y un alcohol. Este compuesto presenta un centro quiral, lo que contribuye a sus propiedades enantioméricas, específicamente la configuración (R). Típicamente es un líquido incoloro a amarillo pálido con un olor agradable, lo que lo hace potencialmente útil en aplicaciones de sabor y fragancia. La presencia del grupo fenilo otorga características aromáticas, mientras que los grupos hidroxilo y butirato contribuyen a su solubilidad en disolventes orgánicos. Etil (R)-2-hidroxi-4-fenilbutirato se estudia a menudo por sus posibles actividades biológicas, incluyendo su papel en diversas rutas sintéticas y sus aplicaciones en productos farmacéuticos. Al igual que muchos compuestos orgánicos, debe manejarse con cuidado, observando los protocolos de seguridad apropiados debido a sus posibles propiedades irritantes. Su estabilidad y reactividad pueden variar dependiendo de las condiciones ambientales, como la temperatura y el pH.

Fórmula: C₁₂H₁₆O₃

InChI: InChI=1/C12H16O3/c1-2-15-12(14)11(13)9-8-10-6-4-3-5-7-10/h3-7,11,13H,2,8-9H2,1H3/t11-/m1/s1

Clave InChI: InChIKey=ZJYKSSGYDPNKQS-LLVKDONJSA-N

SMILES: C(C[C@H](C(OCC)=O)O)C1=CC=CC=C1

Sinónimos:

• (R)-(-)-2-Hydroxy-4-phenylbutyricacidethylester
• (R)-(-)-2-hydroxy-4-phenylbutyrate ethylester
• (R)-2-Hydroxy-4-Phenylbutric Acid Ethyl Ester
• (R)-2-Hydroxy-4-phenylbutanoic acid ethyl ester
• (R)-4-Phenyl-2-hydroxybutanoic acid ethyl ester
• (R)-Ethyl 2-hydroxy-4-phenylbutanoic acid
• (R)-Ethyl 4-phenyl-2-hydroxybutanoate
• (R)-Ethyl2-hydroxy-4-phenylbutanoate
• (R)-ethyl-2-hydroxy-4-phenylbutanoate
• (αR)-α-Hydroxybenzenebutanoic acid ethyl ester
• Benzenebutanoic acid, α-hydroxy-, ethyl ester, (R)-
• Benzenebutanoic acid, α-hydroxy-, ethyl ester, (αR)-
• Ethyl (2R)-2-hydroxy-4-phenylbutyrate
• Ethyl (R)-2-hydroxy-4-phenylbutyrate
• Ethyl (R)-4-phenyl-2-hydroxybutyrate
• Ethyl 2(R)-hydroxy-4-phenylbutyrate
• Ethyl(R)-(-)-2-hydroxy-4-phenyl butyrate
• Ethyl(R)-2-hydroxy-4-phenylbutanoate
• R-2-Hydroxy-4-butylphenyacetate
• R-2-Hydroxy-4-phenyl butyric acid ethyl ester
• ethyl (2R)-2-hydroxy-4-phenylbutanoate
• Ethyl R-2-Hydroxy-4-Phenyl Butanoate
• R-HPBE
• R-2-Hydroxy-4-Phenylbutyric Acid Ethyl Ester
• (R)-2-Hydroxy-4-phenylbutanoicacidethylester
• ETHYL-[(R)-(-)-2-HYDROXY-4-PHENYLBUTYRAT]
• (R )-2-HYDROXY-4-PHENYLBUTYRIC ACID EHTYL ESTER
• Ethyl(R)-2-Hydroxyl-4-PhenylButyrate
• RBZLE
• (R)-(-)-2-HYDROXY-4-PHENYLBUTYRATE ETHYL ESTER
• (R)-ETHYL-4-PHENYL-2-HYDROXYBUTYRATE
• (R)-2-HYDROXY-4-PHENYLBUTYRATE
• R-(-)-ETHYL 2-HYDROXY-4-PHENYLBUTYRATE

Ethyl (R)-(-)-2-hydroxy-4-phenylbutyrate

CAS: 90315-82-5

Fórmula: C₁₂H₁₆O₃

Pureza: 98%

Forma y color: Liquid

Peso molecular: 208.2536

Ref: IN-DA003PZL

Ethyl (R)-2-Hydroxy-4-phenylbutyrate

CAS: 90315-82-5

Ethyl (R)-2-Hydroxy-4-phenylbutyrate

Pureza: 99%

Peso molecular: 208.25g/mol

Ref: 54-OR307153

Ethyl (R)-(-)-2-hydroxy-4-phenylbutyrate

CAS: 90315-82-5

Fórmula: C₁₂H₁₆O₃

Pureza: 98%

Forma y color: Liquid, Viscous

Peso molecular: 208.257

Ref: 10-F011768

(R)-2-Hydroxy-4-phenylbutyric Acid Ethyl Ester

Producto controlado

CAS: 90315-82-5

Applications Used in the preparation of benzothiophenes, benzofurans, and indoles useful in the treatment of insulin resistance and hyperglycemia.
References Chang, A., et al.: Diabetes, 32, 830 (1983), Goldstein, B. et al.: Cell Biochem., 48, 33 (1992), Sredy, J., et al.: Metabolism, 44, 1074 (1995),

Fórmula: C₁₂H₁₆O₃

Forma y color: Neat

Peso molecular: 208.25

Ref: TR-H949096

(R)-2-Hydroxy-4-phenylbutyric acid ethyl ester

CAS: 90315-82-5

(R)-2-Hydroxy-4-phenylbutyric acid ethyl ester is a chiral compound that can be synthesized by an asymmetric synthesis reaction. The compound has been shown to inhibit the enzyme phosphodiesterase, which plays a role in the regulation of cardiac function. (R)-2-Hydroxy-4-phenylbutyric acid ethyl ester has also been shown to induce proliferation of recombinant cells and to bind to monoclonal antibodies against human C5a receptor. It is soluble in organic solvents such as isooctane or pyridine and stable under acidic or basic conditions.

Fórmula: C₁₂H₁₆O₃

Pureza: Min. 95%

Forma y color: Liquid

Peso molecular: 208.25 g/mol

Ref: 3D-FH24269