272451-69-1

Basic information

• Product Name: N~1~-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-methylphenyl]-3-iodo-N~2~-[2-methyl-1-(methylsulfinyl)propan-2-yl]benzene-1,2-dicarboxamide
• Synonyms: 1,2-benzenedicarboxamide, N~2~-[1,1-dimethyl-2-(methylsulfinyl)ethyl]-3-iodo-N~1~-[2-methyl-4-[1,2,2,2-tetrafluoro-1-(trifluoromethyl)ethyl]phenyl]-; N~1~-[4-(1,1,1,2,3,3,3-Heptafluoropropan-2-yl)-2-methylphenyl]-3-iodo-N~2~-[2-methyl-1-(methylsulfinyl)propan-2-yl]phthalamide
• CAS NO: 272451-69-1
• Molecular Formula: C₂₃H₂₂F₇IN₂O₃S
• Molecular Weight: 666.3907
• Mol File: 272451-69-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 567.618°C at 760 mmHg
• Flash Point: 297.085°C
• Density: 1.621g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.568
• CAS DataBase Reference: N~1~-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-methylphenyl]-3-iodo-N~2~-[2-methyl-1-(methylsulfinyl)propan-2-yl]benzene-1,2-dicarboxamide(CAS DataBase Reference)
• NIST Chemistry Reference: N~1~-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-methylphenyl]-3-iodo-N~2~-[2-methyl-1-(methylsulfinyl)propan-2-yl]benzene-1,2-dicarboxamide(272451-69-1)
• EPA Substance Registry System: N~1~-[4-(1,1,1,2,3,3,3-heptafluoropropan-2-yl)-2-methylphenyl]-3-iodo-N~2~-[2-methyl-1-(methylsulfinyl)propan-2-yl]benzene-1,2-dicarboxamide(272451-69-1)

Safety Data

• Hazardous Substances Data: 272451-69-1(Hazardous Substances Data)

Upstream product

• 36567-04-1 2-methyl-1-methylthio-2-propylamine 
• 28418-88-4 3-iodophthalic anhydride 
• 150884-56-3 N-tert-butyloxycarbonyl-3-(4-cyanophenyl)oxaziridine 
• 866639-19-2 3-iodo-N-(1,1-dimethyl-2-methylthioethyl)-o-carbamoylbenzoic acid 
• 371771-07-2 N-(2-methyl-4-heptafluoroisopropylphenyl)-N₂-(1,1-dimethyl-2-methylsulfonylethyl)-(1,2-benzene formamide) 
• 2232-12-4 1,3-Diiodo-5,5-dimethyl-2,4-imidazolidinedione 

Downstream Products

• 272451-65-7 flubendiamide 

Relevant articles and documents

Palladium/carbon catalytic aromatic functional group on the adjacent position iodizate method

The invention discloses a method for iodization of an ortho-position of a functional group on a palladium/carbon catalytic aromatic ring. The method comprises the following steps: mixing an aromatic ring of which a substrate contains a functional group, a

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.