Welcome to LookChem.com Sign In|Join Free
  • or
2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is an organic compound characterized by its unique chemical structure, which features a benzene ring with a bromine atom at the 2nd position, a trifluoromethyl group at the 4th position, and a sulfonyl chloride group attached to the benzene ring. 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is known for its reactivity and is commonly utilized in the synthesis of various organic molecules.

54403-98-4

Post Buying Request

54403-98-4 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

54403-98-4 Usage

Uses

Used in Chemical Synthesis:
2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is used as a synthetic intermediate for the production of various organic compounds. Its reactivity allows it to be a key component in the synthesis of complex molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is used as a building block for the development of new drugs. Its unique structure can be incorporated into drug molecules to enhance their pharmacological properties, such as potency, selectivity, and bioavailability.
Used in Material Science:
2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE can also be used in the field of material science to create novel materials with specific properties. Its incorporation into polymers or other materials can lead to improved characteristics, such as increased stability, enhanced reactivity, or altered physical properties.
Specific Applications:
2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE is used as a reagent for the synthesis of butyl (E)-3-[2-bromo-4-(trifluoromethyl)phenyl]acrylate and 1-benzyl-2-(2-bromo-4-(trifluoromethyl)phenyl)indole. These compounds have potential applications in various fields, such as pharmaceuticals, agrochemicals, and advanced materials.

Check Digit Verification of cas no

The CAS Registry Mumber 54403-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,4,0 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54403-98:
(7*5)+(6*4)+(5*4)+(4*0)+(3*3)+(2*9)+(1*8)=114
114 % 10 = 4
So 54403-98-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrClF3O2S/c8-5-3-4(7(10,11)12)1-2-6(5)15(9,13)14/h1-3H

54403-98-4 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • Alfa Aesar

  • (L19712)  2-Bromo-4-(trifluoromethyl)benzenesulfonyl chloride, 97%   

  • 54403-98-4

  • 1g

  • 478.0CNY

  • Detail
  • Alfa Aesar

  • (L19712)  2-Bromo-4-(trifluoromethyl)benzenesulfonyl chloride, 97%   

  • 54403-98-4

  • 5g

  • 1914.0CNY

  • Detail
  • Aldrich

  • (558427)  2-Bromo-4-(trifluoromethyl)benzenesulfonylchloride  97%

  • 54403-98-4

  • 558427-1G

  • 342.81CNY

  • Detail

54403-98-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-BROMO-4-(TRIFLUOROMETHYL)BENZENESULFONYL CHLORIDE

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:54403-98-4 SDS

54403-98-4Relevant academic research and scientific papers

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

Bheeter, Charles B.,Jin, Rongwei,Bera, Jitendra K.,Dixneuf, Pierre H.,Doucet, Henri

, p. 119 - 124 (2014/03/21)

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

Process for preparing 6H-pyrido[1,2-c][1,3,5]benzothiadiazepines and benzooxadiazepines and derivatives

-

, (2008/06/13)

Compounds of the formula SPC1 Exhibit central nervous system stimulating properties and act as muscle relaxants.

Pyridine containing compounds

-

, (2008/06/13)

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.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 54403-98-4