677007-65-7

Basic information

• Product Name: 1-Propanone, 3-hydroxy-3-(3-methylphenyl)-1-phenyl-
• CAS NO: 677007-65-7
• Molecular Formula: C16H16O2
• Molecular Weight: 240.302
• Mol File: 677007-65-7.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-Propanone, 3-hydroxy-3-(3-methylphenyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanone, 3-hydroxy-3-(3-methylphenyl)-1-phenyl-(677007-65-7)
• EPA Substance Registry System: 1-Propanone, 3-hydroxy-3-(3-methylphenyl)-1-phenyl-(677007-65-7)

Safety Data

• Hazardous Substances Data: 677007-65-7(Hazardous Substances Data)

Usage

Chemical Family

Ketones

Usage

Precursor in the synthesis of various organic compounds

Applications

Building block for pharmaceuticals, fragrances, and other fine chemicals

Properties

Unique structure and properties that make it a valuable tool for organic chemists and researchers in various industries.

Upstream product

• 98-86-2 acetophenone 
• 16619-29-7 phenyl m-methylstyryl ketone 
• 620-23-5 m-tolyl aldehyde 
• 13735-81-4 1-styrenyloxytrimethylsilane 

Downstream Products

• 1054450-24-6 (R)-3-hydroxy-3-(3-methylphenyl)-1-phenylpropan-1-one 
• 16619-29-7 phenyl m-methylstyryl ketone 

Relevant articles and documents

Diastereo- and Enantioselective Catalytic Radical Oxysulfonylation of Alkenes in β,γ-Unsaturated Ketoximes

The asymmetric radical-initiated difunctionalization of internal alkenes, which creates two vicinal stereocenters, has been a significant synthetic challenge despite the tremendous progress achieved for terminal alkenes. This is attributable to the common

PAA-supported Hantzsch 1,4-dihydropyridine ester: An efficient catalyst for the hydrogenation of α,β-epoxy ketones

A new type of water-soluble polymer-supported NADH co-enzyme model-PAA (polyacrylic acid)-supported Hantzsch 1,4-dihydropyridine ester (PAA-HEH) was designed and synthesized. Catalytic amount of the supported reagent was used in the hydrogenation of α,β-epoxy ketones to the corresponding β-hydroxy ketones and showed great catalytic efficiency in the reduction reaction. This PAA-HEH was an optimal potential for recycling use.