54403-98-4

Basic information

• Product Name: 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE
• Synonyms: BUTTPARK 146\11-59;2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE;2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULPHONYL CHLORIDE;2-Bromo-4-(trifluoromethyl)benzenesulphonyl chloride 97%;2-Bromo-4-(trifluoromethyl)benzenesulphonylchloride97%;2-bromo-4-(trifluoromethyl)benzene-1-sulfonyl chloride;2-BROMO-4-(TRIFLUORO;2-broMo-4-(trifluoroMethoxy)benzenesulfonyl chloride
• CAS NO: 54403-98-4
• Molecular Formula: C7H3BrClF3O2S
• Molecular Weight: 323.51
• Product Categories: Organic Building Blocks;Sulfonyl Halides;Sulfur Compounds
• Mol File: 54403-98-4.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 235-236 °C(lit.)
• Flash Point: 95 °F
• Appearance: /
• Density: 1.865 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.00293mmHg at 25°C
• Refractive Index: n20/D 1.5270(lit.)
• Sensitive: Moisture Sensitive
• CAS DataBase Reference: 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE(54403-98-4)
• EPA Substance Registry System: 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE(54403-98-4)

Safety Data

• Hazard Codes: C,Xi
• Statements: 10-34
• Safety Statements: 26-27-36/37/39-45
• RIDADR: UN 2920 8/PG 2
• WGK Germany: 3
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 54403-98-4(Hazardous Substances Data)

Usage

Uses

2-Bromo-4-(trifluoromethyl)benzenesulfonyl chloride may be used to synthesize butyl (E)-3-[2-bromo-4-(trifluoromethyl)phenyl]acrylate and 1-benzyl-2-(2-bromo-4-(trifluoromethyl)phenyl)indole.

InChI:InChI=1/C7H3BrClF3O2S/c8-5-3-4(7(10,11)12)1-2-6(5)15(9,13)14/h1-3H

Upstream product

• 401-78-5 3-bromo-1-trifluoromethylbenzene 

Downstream Products

• 1610527-94-0 1-(2-bromo-4-trifluoromethylbenzenesulfonyl)-3-methylpiperidine 
• 1610528-77-2 3-methyl-1-(4-trifluoromethylbenzenesulfonyl)-1,2,3,4-tetrahydropyridine 
• 1610528-75-0 4-(4-trifluoromethylbenzenesulfonyl)-3,4-dihydro-2H-[1,4]oxazine 
• 1610527-82-6 4-(2-bromo-4-trifluoromethylbenzenesulfonyl)morpholine 
• 1610527-91-7 1-(2-bromo-4-trifluoromethylbenzenesulfonyl)piperidine 
• 1610528-76-1 1-(4-trifluoromethylbenzenesulfonyl)-1,2,3,4-tetrahydropyridine 
• 1349633-06-2 8-{[2-methyl-4-(trifluoromethyl)phenyl]sulfonyl}-2,8-diazaspiro[4.5]decan-1-one 

Relevant articles and documents

Palladium-catalysed dehydrogenative sp3 C-H bonds functionalisation into alkenes: A direct access to N-alkenylbenzenesulfonamides

The palladium-catalysed dehydrogenation of sp3 carbon-hydrogen bonds of N-alkylbenzenesulfonamides allows a simple access to N-alkenylbenzenesulfonamides. The reaction proceeds with easily accessible catalysts, with pivalate as a base, and allo

Pyridine containing compounds

Compounds of the formula SPC1 And tautomers thereof, wherein R, R', R", Z, m and n are as defined hereinafter, exhibit central nervous system stimulating properties and act as muscle relaxants.