CAS 149575-65-5

1,3-Benzothiazole-4-sulfonyl Chloride

Description:

1,3-Benzothiazole-4-sulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group attached to a benzothiazole ring system. This compound typically appears as a solid or crystalline substance and is known for its reactivity, particularly due to the presence of the sulfonyl chloride group, which can undergo nucleophilic substitution reactions. It is often utilized in organic synthesis, particularly in the preparation of sulfonamide derivatives and other functionalized compounds. The compound is soluble in organic solvents, and its reactivity makes it valuable in various chemical applications, including pharmaceuticals and agrochemicals. Safety precautions are essential when handling this substance, as it can be corrosive and may release toxic gases upon reaction with water or moisture. Proper storage conditions are also necessary to maintain its stability and prevent degradation. Overall, 1,3-benzothiazole-4-sulfonyl chloride is a versatile reagent in synthetic organic chemistry.

Formula: C₇H₄ClNO₂S₂

Synonyms:

• 4-Benzothiazolesulfonyl Chloride

1,3-Benzothiazole-4-sulfonyl Chloride

CAS: 149575-65-5

Formula: C₇H₄ClNO₂S₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 233.6952

Ref: IN-DA001LUG

1,3-Benzothiazole-4-sulfonyl chloride

CAS: 149575-65-5

1,3-Benzothiazole-4-sulfonyl chloride

Purity: 95%

Molecular weight: 233.70g/mol

Ref: 54-OR305036

Benzo[d]thiazole-4-sulfonyl chloride

CAS: 149575-65-5

Purity: 98%

Molecular weight: 233.6799927

Ref: 10-F770199

1,3-Benzothiazole-4-sulfonyl Chloride

Controlled Product

CAS: 149575-65-5

Applications 1,3-Benzothiazole-4-sulfonyl Chloride (cas# 149575-65-5) is a compound useful in organic synthesis.
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package

Formula: C₇H₄ClNO₂S₂

Color and Shape: Neat

Molecular weight: 233.70

Ref: TR-B206620