1268607-02-8

Basic information

• Product Name: (E)-1-methyl-4-(3,3,3-trifluoro-2-phenylprop-1-enyl)benzene
• Synonyms: (E)-1-methyl-4-(3,3,3-trifluoro-2-phenylprop-1-enyl)benzene
• CAS NO: 1268607-02-8
• Molecular Weight: 262.274
• Mol File: 1268607-02-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (E)-1-methyl-4-(3,3,3-trifluoro-2-phenylprop-1-enyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-1-methyl-4-(3,3,3-trifluoro-2-phenylprop-1-enyl)benzene(1268607-02-8)
• EPA Substance Registry System: (E)-1-methyl-4-(3,3,3-trifluoro-2-phenylprop-1-enyl)benzene(1268607-02-8)

Safety Data

• Hazardous Substances Data: 1268607-02-8(Hazardous Substances Data)

Upstream product

• 434-45-7 2,2,2-Trifluoroacetophenone 
• 960-16-7 tributylphenylstannane 
• 57297-25-3 1-(4-methoxyphenyl)-2-(4-methylphenyl)ethanone 
• 40739-81-9 p-tolualdehyde p-toluenesulfonylhydrazone 

Relevant articles and documents

Synthesis of (Z)-α-Trifluoromethyl Alkenyl Triflate: A Scaffold for Diverse Trifluoromethylated Species

An efficient method for the synthesis of (Z)-selective α-trifluoromethyl alkenyl triflates is described. As an important fluorinated building block, it is utilized successfully for the synthesis of various trifluoromethyl derivatives such as diarylethylen

One-pot multistep synthesis of trisubstituted alkenes from N -tosylhydrazones and alcohols

A one-pot procedure for the synthesis of trisubstituted alkenes from N-tosylhydrazones and alcohols is reported. This procedure combines the aerobic oxidation reaction and Wittig reaction in one pot, which avoids using of environmentally toxic oxidants and isolation of the intermediates. The simple procedure makes it very attractive for the synthesis of trisubstituted alkenes when alcohols are used as starting materials. A variety of trisubstituted alkenes as well as trifluoromethyl-substituted alkenes were obtained in moderate to good yields (up to 84%) with good E-selectivity (up to 99%). Georg Thieme Verlag Stuttgart.New York.