783-79-9

Basic information

• Product Name: 1,1,1-trifluoro-2-(4-(trifluoromethyl)phenyl)propan-2-ol
• Synonyms: 1,1,1-trifluoro-2-(4-(trifluoromethyl)phenyl)propan-2-ol
• CAS NO: 783-79-9
• Molecular Weight: 258.163
• Mol File: 783-79-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,1,1-trifluoro-2-(4-(trifluoromethyl)phenyl)propan-2-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,1-trifluoro-2-(4-(trifluoromethyl)phenyl)propan-2-ol(783-79-9)
• EPA Substance Registry System: 1,1,1-trifluoro-2-(4-(trifluoromethyl)phenyl)propan-2-ol(783-79-9)

Safety Data

• Hazardous Substances Data: 783-79-9(Hazardous Substances Data)

Upstream product

• 917-64-6 methyl magnesium iodide 
• 74853-66-0 4'-trifluoromethyl-2,2,2-trifluoroacetophenone 
• 421-50-1 1,1,1-trifluoro-2-propanone 
• 402-43-7 p-trifluoromethylphenyl bromide 
• 402-51-7 4-(trifluoromethyl)phenylmagnesium bromide 
• 13329-40-3 4-Iodoacetophenone 
• 120120-26-5 (trifluoromethyl)triethylsilane 
• 709-63-7 1-(4-trifluoromethylphenyl)ethanone 
• 75-46-7 trifluoromethan 
• 111991-14-1 2-(4-trifluoromethylphenyl)oxirane 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 133512-61-5 1,1,1-trifluoro-2-(4-iodophenyl)propan-2-ol 

Downstream Products

• 76954-03-5 1-(4-trifluoromethylphenyl)-1-(trifluoromethyl)ethyl tosylate 
• 122243-16-7 3-Nitro-benzenesulfonic acid 2,2,2-trifluoro-1-methyl-1-(4-trifluoromethyl-phenyl)-ethyl ester 

Relevant articles and documents

Efficient copper-catalyzed trifluoromethylation of aromatic and heteroaromatic iodides: The beneficial anchoring effect of borates

Efficient copper-catalyzed trifluoromethylation of aromatic iodides was achieved with TMSCF3 in the presence of trimethylborate. The Lewis acid was used to anchor the in situ generated trifluoromethyl anion and suppress its rapid decomposition. Broad applicability of the new trifluoromethylating reaction was demonstrated in the functionalization of different aromatic and heteroaromatic iodides.

Efficient synthesis of [18F]trifluoromethane and its application in the synthesis of PET tracers

A new strategy towards [18F]trifluoromethyl-containing compounds is developed. [18F]trifluoromethane is synthesised in a fast and efficient manner and subsequently used in the reaction with aldehydes and ketones forming [18/sup

Substituent effects. XIX. Solvolysis of 1-aryl-1-(trifluoromethyl)ethyl tosylates

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