CAS 74863-82-4

3-Methyl-8-quinolinesulfonyl chloride

Description:

3-Methyl-8-quinolinesulfonyl chloride is an organic compound characterized by its sulfonyl chloride functional group attached to a quinoline ring system. This compound typically appears as a yellow to brown solid and is known for its reactivity, particularly due to the presence of the sulfonyl chloride moiety, which can undergo nucleophilic substitution reactions. It is often used as a reagent in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. The presence of the methyl group at the 3-position of the quinoline ring can influence its chemical reactivity and solubility. Additionally, this compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety precautions should be taken when handling this substance, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or alcohols. Proper storage conditions and protective equipment are essential to ensure safe handling in laboratory settings.

Formula: C₁₀H₈ClNO₂S

InChI: InChI=1S/C10H8ClNO2S/c1-7-5-8-3-2-4-9(15(11,13)14)10(8)12-6-7/h2-6H,1H3

InChI key: InChIKey=XCMAYGDQKTWICK-UHFFFAOYSA-N

SMILES: S(Cl)(=O)(=O)C=1C2=C(C=C(C)C=N2)C=CC1

Synonyms:

• 3-Methylquinoline-3-Sulfonyl Chloride
• 3-Methylquinoline-8-Sulfonyl Chloride
• 3-methyl-8-Quinolinesulfonyl chloride
• 8-Chlorosulfonyl-3-methylquinoline
• 8-Quinolinesulfonyl chloride, 3-methyl-
• 3-Methyl-8-quinolinesulphonyl chloride

3-Methylquinoline-8-sulfonyl chloride

CAS: 74863-82-4

Formula: C₁₀H₈ClNO₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 241.6940

Ref: IN-DA003JRW

3-Methyl-8-quinolinesulphonyl chloride

CAS: 74863-82-4

3-Methyl-8-quinolinesulphonyl chloride

Purity: 98%

Molecular weight: 241.70g/mol

Ref: 54-OR73923

Argatroban Impurity 113

CAS: 74863-82-4

Formula: C₁₀H₈ClNO₂S

Molecular weight: 241.69

Ref: 4Z-A-59131

3-Methyl-8-quinolinesulfonyl chloride

CAS: 74863-82-4

3-Methyl-8-quinolinesulfonyl chloride (3MQSC) is a reaction product of 1,2,4-trioxane and thionyl chloride. 3MQSC is used as an intermediate in the production of l-citrulline from chloroacetic acid. It reacts with paraformaldehyde to form a solid phase synthesis catalyst. 3MQSC catalyzes the reaction between phosphorus pentachloride and chlorine to produce ethyl formate and hydrogen chloride gas. This process is industrialized for the production of ethyl formate, which is used for the manufacture of acetic acid, chlorinated solvents, polymers, and plastics. The high yield of this process makes it one of the most popular routes for producing ethyl formate. Catalysis by 3MQSC can be achieved at low temperature and pressure due to its resistance to heat and low boiling point.

Formula: C₁₀H₈ClNO₂S

Purity: Min. 97 Area-%

Color and Shape: White Yellow Powder

Molecular weight: 241.69 g/mol

Ref: 3D-FM25759

3-Methylquinoline-8-sulfonyl chloride

CAS: 74863-82-4

Formula: C₁₀H₈ClNO₂S

Purity: 95%

Color and Shape: Solid

Molecular weight: 241.69

Ref: 10-F224463

3-Methyl-8-quinolinesulfonyl Chloride

Controlled Product

CAS: 74863-82-4

Stability Moisture Sensitive - Store Under Inert Atmosphere
Applications 3-Methyl-8-quinolinesulfonyl Chloride (cas# 74863-82-4) is a compound useful in organic synthesis.

Formula: C₁₀H₈ClNO₂S

Color and Shape: Neat

Molecular weight: 241.69

Ref: TR-M325967

3-Methyl-8-quinolinesulfonyl Chloride

CAS: 74863-82-4

Formula: C₁₀H₈ClNO₂S

Molecular weight: 241.69

Ref: ST-EA-CP-A123062