1321619-44-6

Basic information

• Product Name: (Z)-methyl 3-(4-methoxyphenyl)-2-(trifluoromethyl)acrylate
• Synonyms: (Z)-methyl 3-(4-methoxyphenyl)-2-(trifluoromethyl)acrylate
• CAS NO: 1321619-44-6
• Molecular Weight: 260.213
• Mol File: 1321619-44-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (Z)-methyl 3-(4-methoxyphenyl)-2-(trifluoromethyl)acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-methyl 3-(4-methoxyphenyl)-2-(trifluoromethyl)acrylate(1321619-44-6)
• EPA Substance Registry System: (Z)-methyl 3-(4-methoxyphenyl)-2-(trifluoromethyl)acrylate(1321619-44-6)

Safety Data

• Hazardous Substances Data: 1321619-44-6(Hazardous Substances Data)

Upstream product

• 382-90-1 methyl α-trifluoromethylacrylate 
• 696-62-8 para-iodoanisole 
• 25245-29-8 5-iodo-1,2,3-trimethoxybenzene 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 105935-24-8 α-trifluoromethylacrylic acid t-butyl ester 
• 67-56-1 methanol 
• 1321619-40-2 (Z)-3-(4-methoxyphenyl)-2-(trifluoromethyl)acrylic acid 
• 104-87-0 4-methyl-benzaldehyde 

Relevant articles and documents

Ligand-free palladium-catalyzed Mizoroki-Heck reaction to synthesize valuable α-trifluoromethylacrylates

α-Trifluoromethylacrylates were synthesized using efficient ligand-free palladium catalyzed Mizoroki-Heck reaction. With the alkyl trifluoromethylacrylates used as substrates, different catalytic systems were explored including Pd/C as a catalyst. Good to excellent yields were obtained with good chemical tolerance.

A synthetic three fluoro methyl acrylic acid derivative method

The invention relates to a novel method for synthesizing a derivative of trifluoromethyl acrylic acid. In the method, a target product with yield of more than 80% can be obtained with commercial trifluoropropionic acid (or esters thereof) and aldehyde as