1569271-96-0

Basic information

• Product Name: (S)-1-(benzo[d][1,3]dioxol-5-yl)-2-(4-chlorophenyl)-2-hydroxyethanone
• Synonyms: (S)-1-(benzo[d][1,3]dioxol-5-yl)-2-(4-chlorophenyl)-2-hydroxyethanone
• CAS NO: 1569271-96-0
• Molecular Weight: 290.703
• Mol File: 1569271-96-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-1-(benzo[d][1,3]dioxol-5-yl)-2-(4-chlorophenyl)-2-hydroxyethanone(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(benzo[d][1,3]dioxol-5-yl)-2-(4-chlorophenyl)-2-hydroxyethanone(1569271-96-0)
• EPA Substance Registry System: (S)-1-(benzo[d][1,3]dioxol-5-yl)-2-(4-chlorophenyl)-2-hydroxyethanone(1569271-96-0)

Safety Data

• Hazardous Substances Data: 1569271-96-0(Hazardous Substances Data)

Upstream product

• 1569272-17-8 (2-(benzo[d][1,3]dioxol-5-yl)-1,3-dithian-2-yl)(4-chlorophenyl)methanone 
• 56579-86-3 2-(3,4-methylenedioxyphenyl)-1,3-dithiane 
• 1569272-08-7 (2-(benzo[d][1,3]dioxol-5-yl)-1,3-dithian-2-yl)(4-chlorophenyl)methanol 
• 120-57-0 piperonal 
• 1569272-28-1 (S)-(2-(benzo[d][1,3]dioxol-5-yl)-1,3-dithian-2-yl)(4-chlorophenyl)methanol 

Relevant articles and documents

Synthesis of chiral α-diarylacetic esters by stereospecific 1,2-aryl migration promoted by in situ generated acetals from benzoins

A simple protocol for the synthesis of α-diarylacetic esters from benzoins is described. In situ generated acetal assists rapid 1,2-aryl migration in a stereospecific manner, paving the way to make enantioenriched α-diarylacetic esters from easily accessi