CAS 17231-95-7

2,3-Dichlorobenzenethiol

Description:

2,3-Dichlorobenzenethiol, with the CAS number 17231-95-7, is an organosulfur compound characterized by the presence of a thiol (-SH) group attached to a benzene ring that has two chlorine substituents at the 2 and 3 positions. This compound typically appears as a colorless to pale yellow liquid with a distinct odor. It is soluble in organic solvents but has limited solubility in water due to its hydrophobic benzene ring. The presence of chlorine atoms enhances its reactivity, making it a useful intermediate in organic synthesis and in the production of various chemical compounds. 2,3-Dichlorobenzenethiol can participate in nucleophilic substitution reactions and can also undergo oxidation to form disulfides or sulfonic acids. Safety considerations are important when handling this compound, as it may pose health risks through inhalation or skin contact, and appropriate precautions should be taken to minimize exposure.

Formula: C₆H₄Cl₂S

InChI: InChI=1S/C6H4Cl2S/c7-4-2-1-3-5(9)6(4)8/h1-3,9H

InChI key: InChIKey=QGRKONUHHGBHRB-UHFFFAOYSA-N

SMILES: ClC1=C(Cl)C=CC=C1S

Synonyms:

• 2,3-Dichlorobenzenethiolate
• 2,3-Dichlorothiophenol
• Benzenethiol, 2,3-dichloro-
• 2,3-Dichlorobenzenethiol

2,3-Dichlorothiophenol

CAS: 17231-95-7

Formula: C₆H₄Cl₂S

Purity: 97%

Color and Shape: Solid

Molecular weight: 179.0670

Ref: IN-DA003FHY

2,3-Dichlorobenzenethiol

CAS: 17231-95-7

Formula: C₆H₄Cl₂S

Purity: >95.0%(GC)

Color and Shape: White to Light yellow to Light orange powder to crystal

Molecular weight: 179.06

Ref: 3B-D1903

2,3-Dichlorothiophenol

CAS: 17231-95-7

2,3-Dichlorothiophenol

Formula: C₆H₄Cl₂S

Purity: 98%

Color and Shape: solid

Molecular weight: 179.07g/mol

Ref: 54-OR30119

2,3-Dichlorothiophenol

CAS: 17231-95-7

Formula: C₆H₄Cl₂S

Purity: 97.0%

Color and Shape: Solid

Molecular weight: 179.06

Ref: 10-F003351

2,3-Dichlorobenzenethiol

CAS: 17231-95-7

2,3-Dichlorobenzenethiol is an organic compound that is used as a reagent in the synthesis of polymers. It inhibits HIV infection by inhibiting viral replication through the inhibition of reverse transcriptase and protease enzymes. This chemical has been used as a standard in analytical methods for estimating the inhibitory effect of substances on these enzymes. 2,3-Dichlorobenzenethiol also has an inhibitory effect on cyclohexane ring formation and polymerization initiation. It is also an important intermediate for the synthesis of naphthalene.

Formula: C₆H₄Cl₂S

Purity: Min. 95%

Molecular weight: 179.06 g/mol

Ref: 3D-SAA23195