42253-99-6

Basic information

• Product Name: (R)-2-PHENYLPROPIONATE ETHYL
• Synonyms: (R)-2-PHENYLPROPIONATE ETHYL;ethyl ester of (S)-(+)-2-phenylpropanoic acid
• CAS NO: 42253-99-6
• Molecular Formula: C₁₁H₁₄O₂
• Molecular Weight: 0
• Mol File: 42253-99-6.mol
• Article Data: 32

Chemical Properties

• Boiling Point: 232.2°C at 760 mmHg
• Flash Point: 93.6°C
• Appearance: /
• Density: 1.012g/cm³
• Vapor Pressure: 0.0597mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: (R)-2-PHENYLPROPIONATE ETHYL(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-PHENYLPROPIONATE ETHYL(42253-99-6)
• EPA Substance Registry System: (R)-2-PHENYLPROPIONATE ETHYL(42253-99-6)

Safety Data

• Hazardous Substances Data: 42253-99-6(Hazardous Substances Data)

Usage

Description

(R)-2-PHENYLPROPIONATE ETHYL is a chemical compound that serves as an ester of (R)-2-phenylpropionic acid and ethanol. It is recognized for its sweet and floral aroma, making it a popular choice in the fragrance and flavor industry.

Uses

Used in Fragrance Industry:
(R)-2-PHENYLPROPIONATE ETHYL is used as a fragrance ingredient for its sweet and floral scent, contributing to the pleasant and long-lasting aroma in perfumes, colognes, and other scented products.
Used in Flavor Industry:
(R)-2-PHENYLPROPIONATE ETHYL is used as a flavoring agent in the food and beverage industry due to its sweet and fruity taste, enhancing the sensory experience of various consumer goods.

InChI:InChI=1/C11H14O2/c1-3-13-11(12)9(2)10-7-5-4-6-8-10/h4-9H,3H2,1-2H3/t9-/m1/s1

Upstream product

• 2406-23-7 (R)-ethyl 2-hydroxy-2-phenylpropanoate 
• 3972-27-8 (R)-2-phenoxy-2-phenyl-propionic acid ethyl ester 
• 24326-78-1 (S)-(+)-α-N.N-Dimethyl-α-phenyl-alaninaethylester 
• 64-17-5 ethanol 
• 492-37-5 hydratropic acid 
• 84028-88-6 ethyl (S)-lactate triflate 
• 71-43-2 benzene 
• 57057-80-4 ethyl (S)-2-[[(4-methylphenyl)sulfonyl]oxy]propanoate 
• 63696-99-1 (S)-ethyl 2-(methylsulfonyloxy)propanoate 
• 7782-24-3 (S)-2-Phenylpropionic acid 
• 62707-19-1 3-ethoxy-2-methyl-3-oxo-2-phenylpropanoic acid 
• 2510-99-8 ethyl 2-phenylpropanoate 
• 111-27-3 hexan-1-ol 
• 55004-59-6 2-bromo-2-phenylpropionic acid ethyl ester 

Downstream Products

• 98-82-8 Isopropylbenzene 
• 7782-24-3 (S)-2-Phenylpropionic acid 
• 7782-26-5 (R)-2-Phenylpropionic acid 
• 1391911-23-1 (R)-4-methyl-N-(2-phenylpropyl)benzenesulfonamide 
• 2510-99-8 ethyl 2-phenylpropanoate 
• 87604-59-9 2-benzyloxy-2-phenyl ethanol 
• 1434644-20-8 C₃₀H₃₃BrN₂O₅S 
• 1434644-15-1 C₁₇H₁₈O₃ 
• 62110-78-5 (S)-(+)-dimethyl (2-oxo-3-phenylbutyl)phosphonate 

Relevant articles and documents

Promotion of multipoint covalent immobilization through different regions of genetically modified penicillin G acylase from E. coli

A novel approach is proposed to prepare a set of immobilized derivatives of a enzyme covalently rigidified through different regions of its surface. Six different variants of penicillin G acylase (PGA) from Escherichia coli (which lacks Cys) were prepared

Synthesis method of (S)-2-aryl propionate compound

The invention discloses a synthesis method of a (S)-2-aryl propionate compound. The (S)-2-aryl propionate compound shown in the formula IV is obtained by taking a compound shown in a formula I and a compound shown in a formula II as raw materials and reacting under the conditions of a chiral ligand shown in a formula III, a nickel catalyst, a photocatalyst, a reducing agent and alkali under the condition of visible light. The method has the advantages of cheap and easily available raw materials, convenient generation, mild conditions, environmental protection and safety, the photocatalyst canbe recycled, the production cost is greatly reduced, the test operation is simple, less waste is generated, and the method can be developed into an industrial production method.

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