1286686-17-6

Basic information

• Product Name: potassium 2,4,6-trimethylphenylsulfonamidomethyltrifluoroborate
• Synonyms: potassium 2,4,6-trimethylphenylsulfonamidomethyltrifluoroborate
• CAS NO: 1286686-17-6
• Molecular Weight: 319.197
• Mol File: 1286686-17-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: potassium 2,4,6-trimethylphenylsulfonamidomethyltrifluoroborate(CAS DataBase Reference)
• NIST Chemistry Reference: potassium 2,4,6-trimethylphenylsulfonamidomethyltrifluoroborate(1286686-17-6)
• EPA Substance Registry System: potassium 2,4,6-trimethylphenylsulfonamidomethyltrifluoroborate(1286686-17-6)

Safety Data

• Hazardous Substances Data: 1286686-17-6(Hazardous Substances Data)

Upstream product

• 773-64-8 2-mesitylenesulphonyl chloride 

Downstream Products

• 321703-41-7 2,4,6-trimethyl-N-(thiophen-2-ylmethyl)benzenesulfonamide 
• 1060352-62-6 2,4,6-trimethyl-N-(thiophen-3-ylmethyl)benzenesulfonamide 
• 311324-55-7 2,4,6-trimethyl-N-(pyridin-3-ylmethyl)benzenesulfonamide 
• 1273318-16-3 N-(4-cyanobenzyl)-2,4,6-trimethylbenzenesulfonamide 
• 1273318-23-2 N-((5-formylfuran-2-yl)methyl)-2,4,6-trimethylbenzenesulfonamide 
• 1273318-22-1 N-((5-acetylthiophen-2-yl)methyl)-2,4,6-trimethylbenzenesulfonamide 
• 1273318-20-9 N-((6-methoxypyridin-3-yl)methyl)-2,4,6-trimethylbenzenesulfonamide 
• 1273318-13-0 N-(4-(1H-pyrrol-1-yl)benzyl)-2,4,6-trimethylbenzenesulfonamide 
• 85045-43-8 N-benzyl-2,4,6-trimethylbenzenesulfonamide 
• 1273318-21-0 N-((6-fluoropyridin-3-yl)methyl)-2,4,6-trimethylbenzenesulfonamide 
• 305849-15-4 N-(4-methoxybenzyl)-2,4,6-trimethylbenzenesulfonamide 
• 677779-64-5 2,4,6-trimethyl-N-(2-methylbenzyl)benzenesulfonamide 
• 305849-14-3 N-(4-fluorobenzyl)-2,4,6-trimethylbenzenesulfonamide 
• 330467-17-9 N-[(2-methoxyphenyl)methyl]-2,4,6-trimethylbenzenesulfonamide 

Relevant articles and documents

Synthesis and cross-coupling of sulfonamidomethyltrifluoroborates

Sulfonamidomethyltrifluoroborates were successfully synthesized and cross-coupled with a wide range of aryl and heteroaryl chlorides, allowing the construction of a sulfonamidomethyl aryl linkage through a new disconnection, thus offering a new way to acc