371771-01-6

Basic information

• Product Name: N₂-[1,1-dimethyl-2-(methylthio)ethyl]-N₁-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-1,2-benzenedicarboxamide
• Synonyms: N₂-[1,1-dimethyl-2-(methylthio)ethyl]-N₁-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-1,2-benzenedicarboxamide
• CAS NO: 371771-01-6
• Molecular Weight: 524.503
• Mol File: 371771-01-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N₂-[1,1-dimethyl-2-(methylthio)ethyl]-N₁-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-1,2-benzenedicarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N₂-[1,1-dimethyl-2-(methylthio)ethyl]-N₁-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-1,2-benzenedicarboxamide(371771-01-6)
• EPA Substance Registry System: N₂-[1,1-dimethyl-2-(methylthio)ethyl]-N₁-{2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl}-1,2-benzenedicarboxamide(371771-01-6)

Safety Data

• Hazardous Substances Data: 371771-01-6(Hazardous Substances Data)

Upstream product

• 238098-26-5 2-methyl-4-(heptafluoropropan-2-yl)-aniline 

Downstream Products

• 371771-07-2 N-(2-methyl-4-heptafluoroisopropylphenyl)-N₂-(1,1-dimethyl-2-methylsulfonylethyl)-(1,2-benzene formamide) 

Relevant articles and documents

PROCESS FOR PRODUCING 2-HALOGENOBENZAMIDE COMPOUND

A novel process for producing a 2-halogenobenzamide compound useful as a raw material or active ingredient for medicines and agricultural chemicals. The process, which is for producing a 2-halogenobenzamide compound represented by the general formula (I): (wherein R1, R2, R3, R4, and R6 may be the same or different and each represents hydrogen or C1-6 alkyl; R5 represents C1-6 alkyl; k is 1 or 2; Y1, Y2, Y3, and Y4 may be the same or different and each represents hydrogen, halogeno, etc.; and X represents chlorine, bromine, or iodine), is characterized by reacting an benzamide compound with a halogenating agent in the presence of a palladium catalyst to obtain a substituted benzamide compound and then reacting the resultant substituted benzamide compound with an oxidizing agent after or without isolating the substituted benzamide compound.