1628200-44-1

Basic information

• Product Name: 1,2-dichloro-4-(1,1,1-trifluorobuta-2,3-dien-2-yl)benzene
• Synonyms: 1,2-dichloro-4-(1,1,1-trifluorobuta-2,3-dien-2-yl)benzene
• CAS NO: 1628200-44-1
• Molecular Weight: 253.051
• Mol File: 1628200-44-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,2-dichloro-4-(1,1,1-trifluorobuta-2,3-dien-2-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-dichloro-4-(1,1,1-trifluorobuta-2,3-dien-2-yl)benzene(1628200-44-1)
• EPA Substance Registry System: 1,2-dichloro-4-(1,1,1-trifluorobuta-2,3-dien-2-yl)benzene(1628200-44-1)

Safety Data

• Hazardous Substances Data: 1628200-44-1(Hazardous Substances Data)

Upstream product

• 220707-94-8 3-(3,4-dichlorophenyl)prop-2-yn-1-ol 
• 1628200-55-4 3-(3,4-dichlorophenyl)prop-2-yn-1-yl 2-bromo-2,2-difluoroacetate 
• 20555-91-3 3,4-dichloroiodobenzene 

Relevant articles and documents

Catalytic One-Step Deoxytrifluoromethylation of Alcohols

A new bench-stable trifluoromethylation reagent, phenyl bromodifluoroacetate, converts readily available alcohols to trifluoromethanes in a Cu-catalyzed deoxytrifluoromethylation reaction. This reaction streamlines access to target biologically active molecules, and should be useful for a variety of medicinal, agricultural, and materials chemists.

Copper-catalyzed decarboxylative trifluoromethylation of propargyl bromodifluoroacetates

The development of efficient methods for accessing fluoA rinated functional groups is desirable. Herein, we report a two step method that utilizes catalytic copper for the decarboxylative trifluoromethylation of propargyl bromodifluoroacetates is described. This protocol affords a mixture of propargyl trifluoromethanes and trifluoromethyl allenes. Georg Thieme Verlag Stuttgart New York.