28049-10-7

Basic information

• Product Name: Benzenepropanoic acid, 2-phenylethyl ester
• CAS NO: 28049-10-7
• Molecular Formula: C17H18O2
• Molecular Weight: 254.329
• Mol File: 28049-10-7.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, 2-phenylethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, 2-phenylethyl ester(28049-10-7)
• EPA Substance Registry System: Benzenepropanoic acid, 2-phenylethyl ester(28049-10-7)

Safety Data

• Hazardous Substances Data: 28049-10-7(Hazardous Substances Data)

Upstream product

• 60-12-8 2-phenylethanol 
• 501-52-0 3-Phenylpropionic acid 
• 3070-40-4 β-phenylpropionyl peroxide 
• 74783-34-9 3,3,6,6-tetra(phenethyl)-1,2,4,5-tetraoxan 
• 103-25-3 3-phenylpropanoic acid methyl ester 
• 23522-73-8 3-phenylpropionic acid 4-chlorophenyl ester 
• 1104567-97-6 2-(3-phenylpropionyloxy)benzothiazole 
• 124552-55-2 N-(3-phenylpropionyloxy)benzotriazole 
• 84379-71-5 1,3-dioxoisoindolin-2-yl 3-phenylpropanoate 
• 179386-76-6 1-(1H-benzotriazol-1-yl)-3-phenylpropan-1-one 
• 100-42-5 styrene 
• 141-53-7 sodium formate 
• 107978-04-1 3-(1-oxo-3-phenylpropyl)-1,3-oxazolidin-2-one 
• 710-11-2 2-oxo-4-phenylbutyric acid 

Relevant articles and documents

Lipase-catalyzed esterification in water enabled by nanomicelles. Applications to 1-pot multi-step sequences

Esterification in an aqueous micellar medium is catalyzed by a commercially available lipase in the absence of any co-factors. The presence of only 2 wt% designer surfactant, TPGS-750-M, assists in a 100% selective enzymatic process in which only primary alcohols participate (in a 1?:?1 ratio with carboxylic acid). An unexpected finding is also disclosed where the simple additive, PhCF3 (1 equiv. vs. substrate), appears to significantly extend the scope of usable acid/alcohol combinations. Taken together, several chemo- and bio-catalyzed 1-pot, multi-step reactions can now be performed in water.

Esterification or Thioesterification of Carboxylic Acids with Alcohols or Thiols Using Amphipathic Monolith-SO3H Resin

We have developed a method for the esterification of carboxylic acids with alcohols using amphipathic, monolithic-resin bearing sulfonic acid moieties as cation exchange functions (monolith-SO3H). Monolith-SO3H efficiently catalyzed the esterification of aromatic and aliphatic carboxylic acids with various primary and secondary alcohols (1.55.0 equiv) in toluene at 6080 °C without the need to remove water generated during the reaction. The amphipathic property of monolith-SO3H facilitates dehydration due to its capacity for water absorption. This reaction was also applicable to thioesterification, wherein the corresponding thioesters were obtained in excellent yield using only 2.0 equiv of thiol in toluene, although heating at 120 °C was required. Moreover, monolith-SO3H was separable from the reaction mixtures by simple filtration and reused for at least five runs without decreasing the catalytic activity.

Method for selective reduction α, β - unsaturated carbonyl compound carbon-carbon double bond (by machine translation)

The invention discloses a method for selectively reducing carbon-carbon double bonds in α and β - unsaturated carbonyl compounds, which comprises the following steps of adding α, β - unsaturated carbonyl compounds shown in formula (I) in an electrolysis system and reducing α and β - unsaturated carbonyl compounds with carbonyl-conjugated carbon-carbon double bonds through an electrochemical cathodic reduction reaction. Compared with the reported method, the method disclosed by the invention does not use a metal catalyst and an external oxidant; and the reaction raw material and the electrolyte are low in price, nontoxic and tasteless, simple and convenient in post-treatment. (by machine translation)