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

• 74783-34-9 3,3,6,6-tetra(phenethyl)-1,2,4,5-tetraoxan 
• 3070-40-4 β-phenylpropionyl peroxide 
• 60-12-8 2-phenylethanol 
• 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 
• 501-52-0 3-Phenylpropionic acid 
• 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 
• 621-82-9 Cinnamic acid 
• 63238-64-2 3-phenylacrylic acid phenethyl ester 

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.

Development of a triazinedione-based dehydrative condensing reagent containing 4-(dimethylamino)pyridine as an acyl transfer catalyst

A new triazinedione-based reagent, (N,N′-dialkyl)triazinedione-4-(dimethylamino)pyridine (ATD-DMAP) was developed for the operationally simple dehydrative condensation of carboxylic acids. This reagent comprises an ATD core and DMAP as the leaving group, which is liberated into the reaction system to accelerate acyl transfer reactions. Upon adding ATD-DMAP to a mixture of carboxylic acids and alcohols in the presence of an amine base, the corresponding esters were formed rapidly at room temperature. Moreover, dehydrative condensation between carboxylic acids and amines using ATD-DMAP proceeded in high yield.

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)