CAS 65433-99-0

6-Quinolinesulfonyl chloride

Description:

6-Quinolinesulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group attached to a quinoline ring system. It typically appears as a yellow to brown solid or liquid, depending on its purity and form. This compound is known for its reactivity, particularly due to the presence of the sulfonyl chloride group, which can participate in nucleophilic substitution reactions. It is often used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The compound is soluble in organic solvents such as dichloromethane and chloroform but is generally insoluble in water. Safety precautions are essential when handling this substance, as it can be corrosive and may cause irritation to the skin, eyes, and respiratory system. Proper storage in a cool, dry place away from moisture and incompatible substances is recommended to maintain its stability and reactivity.

Formula: C₉H₆ClNO₂S

InChI: InChI=1/C9H6ClNO2S/c10-14(12,13)8-3-4-9-7(6-8)2-1-5-11-9/h1-6H

SMILES: c1cc2cc(ccc2nc1)S(=O)(=O)Cl

Synonyms:

• Quinoline-6-Sulfonyl Chloride
• 6-Quinolinesulfonyl chloride
• 6-Quinolinesulfonyl chloride, 90+%

Quinoline-6-sulfonyl chloride

CAS: 65433-99-0

Formula: C₉H₆ClNO₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 227.6674

Ref: IN-DA00EETM

Quinoline-6-sulfonyl chloride

CAS: 65433-99-0

Quinoline-6-sulfonyl chloride

Purity: 95%

Molecular weight: 227.67g/mol

Ref: 54-OR79206

Quinoline-6-sulfonyl chloride

CAS: 65433-99-0

Formula: C₉H₆ClNO₂S

Purity: 95%

Molecular weight: 227.66

Ref: 10-F053183

Quinoline-6-sulfonyl chloride

CAS: 65433-99-0

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Formula: C₉H₆ClNO₂S

Purity: Min. 95%

Molecular weight: 227.67 g/mol

Ref: 3D-FQ27387