351-81-5

Basic information

• Product Name: Acetamide, N-[4-[(trifluoromethyl)thio]phenyl]-
• CAS NO: 351-81-5
• Molecular Formula: C9H8F3NOS
• Molecular Weight: 235.23
• Mol File: 351-81-5.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: Acetamide, N-[4-[(trifluoromethyl)thio]phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Acetamide, N-[4-[(trifluoromethyl)thio]phenyl]-(351-81-5)
• EPA Substance Registry System: Acetamide, N-[4-[(trifluoromethyl)thio]phenyl]-(351-81-5)

Safety Data

• Hazardous Substances Data: 351-81-5(Hazardous Substances Data)

Upstream product

• 372-16-7 thioorthocarbonotrifluoridic acid 4-amino-phenyl ester 
• 887144-94-7 Togni's reagent II 
• 99893-78-4 pent-4-en-1-yl 4-chlorobenzoate 
• 1126-81-4 4-acetamidothiophenol 
• 2926-29-6 Langlois reagent 
• 622-50-4 4-Acetamido-1-iodobenzene 
• 3872-23-9 Copper(I) trifluoromethanethiolate 
• 122-80-5 N-acetyl-p-phenylenediamine 
• 101251-09-6 (4-acetylaminophenyl)boronic acid 
• 2314-97-8 iodotrifluoromethane 
• 713-66-6 4-nitrophenyl trichloromethylsulfide 
• 403-66-7 p-nitrophenyl trifluoromethyl sulfide 
• 701-57-5 1-methylthio-4-nitro-benzene 
• 887144-97-0 Togni's reagent 

Downstream Products

• 1948-04-5 N-(4-((trifluoromethyl)sulfinyl)phenyl)acetamide 
• 448-41-9 N-{2-nitro-4-[(trifluoromethyl)sulfanyl]phenyl}acetamide 
• 324-13-0 N,N'-(4-trifluoromethylsulfanyl-o-phenylene)-bis-acetamide 
• 404-74-0 2-nitro-4-trifluoromethylsulfanyl-aniline 
• 370-46-7 4-trifluoromethylsulfanyl-o-phenylenediamine 
• 393-88-4 2,3-diphenyl-6-trifluoromethylsulfanyl-quinoxaline 
• 588-81-8 thioacetic acid-(4-trifluoromethylsulfanyl-anilide) 

Relevant articles and documents

Togni-II Reagent Mediated Selective Hydrotrifluoromethylation and Hydrothiolation of Alkenes?

Based on the redox reactions of Togni-II reagent and thiols, a thiol-tuned selective functionalization of unactivated olefins was disclosed. In combination with aryl thiols, stoichiometric amount of Togni-II reagent prompted a hydrotrifluoromethylation of alkenes, in which, aryl thiols played as reductant and hydrogen source; while by utilization of alkyl thiols, catalytic amount of Togni-II reagent initiated thiol-ene and thiol-yne reactions. The reported applications are characterized by their operational simplicity and wide functional group tolerance.

PEST CONTROL COMPOSITION AND USE THEREFOR

PROBLEM TO BE SOLVED: To provide a pest control composition having an excellent control effect on pests such as ixodid and flea. SOLUTION: A pest control composition contains a condensed heterocyclic compound represented by formula (1), and at least one p

Trifluoromethylthiolation of Unsymmetrical λ3-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF3 Group

The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward pathway for the synthesis of aryl trifluoromethyl thioethers under mild reaction conditions and within short reaction times. High chemoselectivity was achieved by using mesityl as a leaving group. A large range of novel [(het)aryl](mesityl)iodonium salts underwent this reaction under the optimized conditions to give the desired products in moderate to good yields.