CAS 23378-88-3

3,5-Dichloro-2-hydroxybenzenesulfonyl chloride

Description:

3,5-Dichloro-2-hydroxybenzenesulfonyl chloride, with the CAS number 23378-88-3, is an organic compound characterized by its sulfonyl chloride functional group, which is known for its reactivity in various chemical reactions. This compound features a benzene ring substituted with two chlorine atoms at the 3 and 5 positions, and a hydroxyl group at the 2 position, contributing to its unique chemical properties. The presence of the sulfonyl chloride group makes it a potent electrophile, allowing it to participate in nucleophilic substitution reactions, particularly with amines and alcohols. It is typically used in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The compound is generally handled with care due to its potential to release hydrochloric acid upon hydrolysis, and it may pose health risks if inhaled or if it comes into contact with skin. Proper safety measures, including the use of personal protective equipment, are essential when working with this substance in a laboratory setting.

Formula: C₆H₃Cl₃O₃S

InChI: InChI=1S/C6H3Cl3O3S/c7-3-1-4(8)6(10)5(2-3)13(9,11)12/h1-2,10H

InChI key: InChIKey=KXFQRJNVGBIDHA-UHFFFAOYSA-N

SMILES: S(Cl)(=O)(=O)C1=C(O)C(Cl)=CC(Cl)=C1

Synonyms:

• 2,4-Dichlorophenol-6-sulfonyl chloride
• 2-Hydroxy-3,5-dichlorobenzenesulfonyl chloride
• 2-Hydroxy-3,5-dichlorophenylsulfonyl chloride
• 3,5-Dichloro-2-hydroxybenzene-1-sulfonyl chloride
• 3,5-Dichloro-2-hydroxybenzenesulphonyl chloride
• 3,5-Dichloro-2-hydroxyphenylsulfonyl chloride
• 3,5-Dichloro-6-hydroxybenzenesulfonyl chloride
• Benzenesulfonyl chloride, 3,5-dichloro-2-hydroxy-
• 3,5-Dichloro-2-hydroxybenzenesulfonyl chloride

3,5-Dichloro-2-hydroxybenzenesulfonyl chloride, 97%

CAS: 23378-88-3

3,5-Dichloro-2-hydroxybenzenesulfonyl chloride is used in the synthesis of (1R,2R)-(+)-1,2-(3,3?,5,5?-tetrachloro-2,2?-dihydroxydibenzenesulfonamido)-1,2-diphenylethane1 and (1R,2R)-(+)- 1,2-(3,3?,5,5?-tetrachloro-2,2?-dihydroxydibenzenesulfonamido)cyclohexane. It was used as chromogenic system in o

Formula: C₆H₃Cl₃O₃S

Purity: 97%

Color and Shape: Crystals or powder or crystalline powder or lumps, White to cream to pale brown

Molecular weight: 261.50

Ref: 02-L12147

Benzenesulfonyl chloride, 3,5-dichloro-2-hydroxy-

CAS: 23378-88-3

Formula: C₆H₃Cl₃O₃S

Purity: 98%

Color and Shape: Solid

Molecular weight: 261.5102

Ref: IN-DA002N12

3,5-Dichloro-2-Hydroxybenzenesulfonyl Chloride

CAS: 23378-88-3

3,5-Dichloro-2-Hydroxybenzenesulfonyl Chloride

Purity: 95%

Molecular weight: 261.51g/mol

Ref: 54-OR1030504

3,5-Dichloro-2-hydroxybenzene-1-sulfonyl chloride

CAS: 23378-88-3

Purity: 98%

Molecular weight: 261.5

Ref: 10-F671132

2,4-Dichlorophenol-6-sulphonyl chloride

CAS: 23378-88-3

2,4-Dichlorophenol-6-sulphonyl chloride (2,4-DCP) is a molecule that has been shown to have antibacterial activity against Gram-positive and Gram-negative bacteria. It inhibits the growth of bacteria by binding to the cell wall and inhibiting enzyme activity. 2,4-DCP also has hemolytic activity in vitro. The mechanism of this effect is not well understood but may involve an interaction with membrane lipids or proteins in red blood cells. In addition, 2,4-DCP has been shown to inhibit the growth of staphylococcus and other bacterial strains in vitro. The inhibition of bacterial growth by 2,4-DCP is reversible with exposure to hydrated conditions.

Formula: C₆H₃Cl₃O₃S

Purity: Min. 95%

Molecular weight: 261.51 g/mol

Ref: 3D-FD70372