10375-45-8

Basic information

• Product Name: 1,3-diphenyl-2-(1-phenylprop-2-ynyl)-propane-1,3-dione
• Synonyms: 1,3-diphenyl-2-(1-phenylprop-2-ynyl)-propane-1,3-dione
• CAS NO: 10375-45-8
• Molecular Weight: 338.406
• Mol File: 10375-45-8.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1,3-diphenyl-2-(1-phenylprop-2-ynyl)-propane-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-diphenyl-2-(1-phenylprop-2-ynyl)-propane-1,3-dione(10375-45-8)
• EPA Substance Registry System: 1,3-diphenyl-2-(1-phenylprop-2-ynyl)-propane-1,3-dione(10375-45-8)

Safety Data

• Hazardous Substances Data: 10375-45-8(Hazardous Substances Data)

Upstream product

• 16169-88-3 1-phenylprop-2-ynyl acetate 
• 120-46-7 1,3-diphenylpropanedione 
• 4187-87-5 1-Phenyl-2-propyn-1-ol 

Downstream Products

• 1122593-67-2 (5-methyl-2,4-diphenylfuran-3-yl)(phenyl)methanone 
• 10375-46-9 1,3-diphenyl-2-(1-phenylpropyl)propane-1,3-dione 

Relevant articles and documents

Gold-catalyzed addition of carbon nucleophiles to propargyl carboxylates

Propargyl carboxylates react with 1,3-dicarbonyl compounds and electron-rich arenes in the presence of Au(l) catalysts to give enol carboxylates via α,β-unsaturated Au(l) carbenes or Au(l)-coordinated alienes formed by 1,2- or 1,3-acyl migration, respecti

SnCl2-catalyzed propargylic substitution of propargylic alcohols with carbon and nitrogen nucleophiles

A weak Lewis acid, tin(II) chloride, which is insensitive to water and air, functioned as a catalyst for the propargylic substitution of secondary propargylic alcohols with carbon nucleophiles, such as electron-rich arenes, heteroarenes, and 1,3-dicarbony

Bronsted acid catalyzed propargylation of 1,3-dicarbonyl derivatives. Synthesis of tetrasubstituted furans

Simple Bronsted acids such as p-toluenesulfonic acid monohydrate (PTS) efficiently catalyze a direct substitution of the hydroxyl group in propargylic alcohols with 1,3-dicarbonyl compounds. Selective propargylation or allenylation is obtained depending o