38574-62-8

Basic information

• Product Name: methyl (S)-(+)-2-benzylpropionate
• Synonyms: methyl (S)-(+)-2-benzylpropionate
• CAS NO: 38574-62-8
• Molecular Weight: 178.231
• Mol File: 38574-62-8.mol
• Article Data: 75

Chemical Properties

• CAS DataBase Reference: methyl (S)-(+)-2-benzylpropionate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (S)-(+)-2-benzylpropionate(38574-62-8)
• EPA Substance Registry System: methyl (S)-(+)-2-benzylpropionate(38574-62-8)

Safety Data

• Hazardous Substances Data: 38574-62-8(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 141543-31-9 (2-Benzyl-cyclopropylmethyl)-dimethyl-phenyl-silane 
• 1007-32-5 benzyl ethyl ketone 
• 300-57-2 allylbenzene 
• 201230-82-2 carbon monoxide 
• 186581-53-3 diazomethane 
• 1009-67-2 2-methyl-3-phenylpropanoic acid 
• 1009-67-2 2-methyl-3-phenylpropionic acid 
• 29393-16-6 methyl 2-methyl-3-phenylpropionate 
• 591-50-4 iodobenzene 
• 753016-42-1 ((S)-1-Methoxy-2-methyl-cyclopropoxy)-trimethyl-silane 
• 5445-77-2 2-benzylpropionaldehyde 
• 616-38-6 carbonic acid dimethyl ester 
• 101-39-3 2-methyl-3-phenyl-2-propenal 

Downstream Products

• 14367-67-0 2-methyl-3-phenylpropionic acid 
• 29393-16-6 methyl (2R)-2-methyl-3-phenylpropanoate 
• 123820-51-9 ((Z)-1-Methoxy-2-methyl-3-phenyl-propenyloxy)-trimethyl-silane 
• 1328064-88-5 2,2-dimethyl-3-phenyl-N-(quinolin-8-yl)propanamide 
• 62931-24-2 2,2-dimethyl-3-phenylpropanoyl chloride 
• 5669-14-7 2,2-dimethyl-3-phenylpropanoic acid 

Relevant articles and documents

The unexpected kinetic effect of enzyme mixture: The case of enzymatic esterification

During the studies towards synthesis of carboxylic acids esters, using ethyl carbonate and carboxylic acid as substrates, we found that different single enzyme systems provide model ethyl 3-phenylpropanoate in very low yield. Systematic studies proved tha

Electrochemically Enabled, Nickel-Catalyzed Dehydroxylative Cross-Coupling of Alcohols with Aryl Halides

As alcohols are ubiquitous throughout chemical science, this functional group represents a highly attractive starting material for forging new C-C bonds. Here, we demonstrate that the combination of anodic preparation of the alkoxy triphenylphosphonium ion and nickel-catalyzed cathodic reductive cross-coupling provides an efficient method to construct C(sp2)-C(sp3) bonds, in which free alcohols and aryl bromides - both readily available chemicals - can be directly used as coupling partners. This nickel-catalyzed paired electrolysis reaction features a broad substrate scope bearing a wide gamut of functionalities, which was illustrated by the late-stage arylation of several structurally complex natural products and pharmaceuticals.

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A fungicidal composition comprising a mixture of components (A) and (B), wherein component (A) is a 8-fluoroquinoline-3-carboxamide of formula I and component (B) is selected from the group consisting of pydiflumetofen, benzovindiflupyr, difenoconazole, hexaconazole, azoxystrobin, fludioxonil, cyprodinil, fluazinam, isopyrazam, pyroquilon, tricyclazole, chlorothalonil, propiconazole, aminopyrifen, penconazole, prothioconazole, mancozeb, fenproprimorph, fenpropidin, sulphur and Bacillus subtilis strains, as well as to the use of the compositions in agriculture or horticulture for controlling or preventing infestation of plants by phytopathogenic microorganisms, preferably, fungi.