115377-82-7

Basic information

• Product Name: 2-oxo-1,2-di-p-tolylethyl benzoate
• Synonyms: 2-oxo-1,2-di-p-tolylethyl benzoate
• CAS NO: 115377-82-7
• Molecular Weight: 344.41
• Mol File: 115377-82-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-oxo-1,2-di-p-tolylethyl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: 2-oxo-1,2-di-p-tolylethyl benzoate(115377-82-7)
• EPA Substance Registry System: 2-oxo-1,2-di-p-tolylethyl benzoate(115377-82-7)

Safety Data

• Hazardous Substances Data: 115377-82-7(Hazardous Substances Data)

Upstream product

• 104-87-0 4-methyl-benzaldehyde 
• 1218-89-9 4,4'-dimethylbenzoin 
• 98-88-4 benzoyl chloride 
• 110212-00-5 5-benzoyl-4,5-dihydro-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine-4-carbonitrile 
• 116943-91-0 5-benzoyl-4,5-dihydro-6-methyl-1-phenyl-1H-pyrazolo<3,4-d>pyrimidine-4-carbonitrile 

Downstream Products

• 16178-22-6 2-phenyl-4,5-bis-(4-trans-styryl-phenyl)-oxazole 
• 16178-23-7 4,5-bis-[4-(trans-2-biphenyl-4-yl-vinyl)-phenyl]-2-phenyl-oxazole 
• 16178-24-8 4,5-bis-[4-(trans-2-naphthalen-1-yl-vinyl)-phenyl]-2-phenyl-oxazole 
• 51490-06-3 1,2-di-p-tolyl-ethanone 
• 16112-17-7 2-phenyl-4,5-(di-p-tolyl)oxazole 

Relevant articles and documents

Palladium-Catalyzed Chemo- and Enantioselective C?O Bond Cleavage of α-Acyloxy Ketones by Hydrogenolysis

A chemoselective C?O bond cleavage of the ester alkyl side-chain of α-acyloxy ketones was realized for the first time by a highly efficient palladium-catalyzed hydrogenolysis (S/C=6000, the highest catalytic efficiency by far). Furthermore, a kinetic resolution of α-acyloxy ketones was first developed by enantioselective hydrogenolysis with good yields and up to 99 % ee.

Studies on pyrazolo[3,4-d]pyrimidine derivatives. XVII. Reactions of 5-benzoyl-4,5-dihydro-6-methyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine-4- carbonitrile (The 6-methylpyrazolopyrimidine Reissert compound)

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