CAS 223671-80-5

7-Isoquinolinesulfonylchloride, 1,4-dichloro-

Description:

7-Isoquinolinesulfonylchloride, 1,4-dichloro- is a chemical compound characterized by its sulfonyl chloride functional group attached to an isoquinoline structure. 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 participate in nucleophilic substitution reactions. The dichloro substituents on the isoquinoline ring enhance its electrophilic properties, making it useful in various synthetic applications, including the preparation of sulfonamide derivatives and other complex organic molecules. It is important to handle this compound with care, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or amines. In laboratory settings, it is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Proper safety protocols should be followed when working with this compound, including the use of personal protective equipment and working in a well-ventilated area or fume hood.

Formula: C₉H₄Cl₃NO₂S

Synonyms:

• 1,4-Dichloro-7-isoquinolinesulfonylchloride

1,4-Dichloroisoquinoline-7-sulfonyl chloride

CAS: 223671-80-5

1,4-Dichloroisoquinoline-7-sulfonyl chloride

Purity: 97%

Ref: 54-OR1039568

7-ISOQUINOLINESULFONYL CHLORIDE, 1,4-DICHLORO-

CAS: 223671-80-5

Formula: C₉H₄Cl₃NO₂S

Purity: 97%

Molecular weight: 296.55

Ref: 10-F534814

1,4-Dichloro-7-isoquinolinesulfonyl Chloride

Controlled Product

CAS: 223671-80-5

Applications Intermediate of isoquinolinylguanidines as urokinase inhibitors.
References Rachlin, S., et al.: J. Med. Chem., 23, 13 (1980), Bridges, A., et al.: Bioorg. Med. Chem., 1, 403 (1993), Palolahti, M; Exp Dermatol 1993, 2, 29 (1993), Wendt, M., et al.: Bioorg. Med. Chem. Lett., 14, 3063 (2004),

Formula: C₉H₄Cl₃NO₂S

Color and Shape: Neat

Molecular weight: 296.56

Ref: TR-D434950