76886-35-6

Basic information

• Product Name: 3-(benzyloxy)-2-methyl-1-phenylpropan-1-one
• Synonyms: 3-(benzyloxy)-2-methyl-1-phenylpropan-1-one
• CAS NO: 76886-35-6
• Molecular Weight: 254.329
• Mol File: 76886-35-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(benzyloxy)-2-methyl-1-phenylpropan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(benzyloxy)-2-methyl-1-phenylpropan-1-one(76886-35-6)
• EPA Substance Registry System: 3-(benzyloxy)-2-methyl-1-phenylpropan-1-one(76886-35-6)

Safety Data

• Hazardous Substances Data: 76886-35-6(Hazardous Substances Data)

Upstream product

• 3587-60-8 Benzyloxymethyl chloride 
• 37471-46-8 1-phenyl-1-trimethylsiloxypropene 
• 93-55-0 1-phenyl-propan-1-one 
• 2749-70-4 bis(benzyloxy)methane 
• 71268-59-2 (E)-1-phenyl-1-(trimethylsiloxy)propene 
• 66323-99-7 trimethyl[(Z)-(1-phenyl-1-propenyl)oxy]silane 

Downstream Products

• 22661-04-7 (2SR,3SR)-2-methyl-3-phenylbutan-1-ol 

Relevant articles and documents

Alkyl Ethers as Traceless Hydride Donors in Br?nsted Acid Catalyzed Intramolecular Hydrogen Atom Transfer

A new protocol for the deoxygenation of alcohols and the hydrogenation of alkenes under Br?nsted acid catalysis has been developed. The method is based on the use of either a benzyl or isopropyl ether as a traceless hydrogen-atom donor, and involves an intramolecular hydride transfer as a key step, which is achieved in a regio- and stereoselective manner.

TRIMETHYLSILYL TRIFLATE IN ORGANIC SYNTHESIS

Trimethylsilyl triflate is a powerful silylating agent for organic compounds and acts as a catalyst which accelerates a variety of nucleophilic reactions in aprotic media.The reactions proceed via one-center, electrophilic coordination of the silyl group to hetero functional groups and exhibit unique selectivities.