351536-34-0

Basic information

• Product Name: 1,1,1-trichloro-4-p-tolyl-but-3-en-2-ol
• Synonyms: 1,1,1-trichloro-4-p-tolyl-but-3-en-2-ol
• CAS NO: 351536-34-0
• Molecular Weight: 265.567
• Mol File: 351536-34-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1,1,1-trichloro-4-p-tolyl-but-3-en-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,1-trichloro-4-p-tolyl-but-3-en-2-ol(351536-34-0)
• EPA Substance Registry System: 1,1,1-trichloro-4-p-tolyl-but-3-en-2-ol(351536-34-0)

Safety Data

• Hazardous Substances Data: 351536-34-0(Hazardous Substances Data)

Upstream product

• 67-66-3 chloroform 
• 56578-35-9 4-methyl-cinnamaldehyde 
• 20754-20-5 3-p-tolyl-acrylic acid methyl ester 
• 1866-39-3 trans-p-methylcinnamic acid 
• 122058-30-4 p-methylcinnamyl alcohol 
• 650-51-1 sodium trichloroacetate 
• 351536-15-7 2-tert-butyldimethylsilyloxy-1,1,1-trichloro-4-p-tolyl-3-butene 

Downstream Products

• 1280199-15-6 (E)-1,1,1-trichloro-4-p-tolylbut-3-en-2-one 
• 351536-15-7 2-tert-butyldimethylsilyloxy-1,1,1-trichloro-4-p-tolyl-3-butene 

Relevant articles and documents

Highly enantioselective synthesis of α-trichloromethyldihydropyrans catalyzed by bifunctional organocatalysts

The enantioselective Michael addition of α-cyanoketones to α,β-unsaturated trichloromethyl ketones was firstly reported. With a phenylalanine-derived bifunctional piperazine/thiourea catalyst, a series of α-trichloromethyldihydropyrans were obtained with