CAS 54429-56-0

2-Bromoethanesulfonyl chloride

Description:

2-Bromoethanesulfonyl chloride, with the CAS number 54429-56-0, is an organic compound characterized by the presence of both a bromine atom and a sulfonyl chloride functional group. It typically appears as a colorless to pale yellow liquid and is known for its reactivity, particularly in nucleophilic substitution reactions. The sulfonyl chloride group makes it a potent electrophile, allowing it to readily react with nucleophiles such as amines and alcohols, which can lead to the formation of sulfonamides or sulfonate esters. This compound is often utilized in organic synthesis, particularly in the preparation of sulfonamide derivatives and other functionalized compounds. Due to its reactive nature, it should be handled with care, as it can be corrosive and may pose health hazards upon exposure. Proper safety measures, including the use of personal protective equipment and working in a well-ventilated area or fume hood, are essential when working with this substance.

Formula: C₂H₄BrClO₂S

InChI: InChI=1S/C2H4BrClO2S/c3-1-2-7(4,5)6/h1-2H2

InChI key: InChIKey=FPJOBRDFPQKHLI-UHFFFAOYSA-N

SMILES: C(S(Cl)(=O)=O)CBr

Synonyms:

• 2-Bromo-ethanesulfonyl chloride
• 2-Bromoethane-1-sulfonyl chloride
• 2-Bromoethanesulfonyl chloride
• Ethanesulfonyl chloride, 2-bromo-

2-Bromoethanesulfonyl Chloride

CAS: 54429-56-0

Formula: C₂H₄BrClO₂S

Purity: 97%

Color and Shape: Liquid

Molecular weight: 207.4740

Ref: IN-DA003GRU

2-Bromoethanesulfonyl Chloride

CAS: 54429-56-0

2-Bromoethanesulfonyl Chloride

Purity: 98%

Molecular weight: 207.47g/mol

Ref: 54-OR1010362

2-BROMOETHANESULFONYL CHLORIDE

CAS: 54429-56-0

Formula: C₂H₄BrClO₂S

Purity: 97%

Color and Shape: Liquid

Molecular weight: 207.47

Ref: 10-F387448

2-Bromoethanesulfonyl chloride

CAS: 54429-56-0

2-Bromoethanesulfonyl chloride is an aminoglycoside antibiotic that has been shown to be activated by conjugation with amines. This agent is a potent drug, which inhibits bacterial growth and has been shown to be effective against some strains of bacteria that are resistant to other antibiotics such as sulfonamides. 2-Bromoethanesulfonyl chloride binds to the enzyme ribosomal protein S12 and blocks protein synthesis in bacteria cells by preventing the formation of peptide bonds between amino acids. It also inhibits production of purine nucleotides and adenosine triphosphate (ATP) in bacterial cells. 2-Bromoethanesulfonyl chloride may also inhibit cell division by binding to DNA gyrase, resulting in the accumulation of single-stranded DNA which causes DNA degradation.

Formula: C₂H₄BrClO₂S

Purity: Min. 95%

Molecular weight: 207.47 g/mol

Ref: 3D-ECA42956