CAS 1706462-05-6

4-[(Phenylmethyl)sulfonyl]butanoyl chloride

Description:

4-[(Phenylmethyl)sulfonyl]butanoyl chloride, identified by its CAS number 1706462-05-6, is an organic compound characterized by the presence of a butanoyl chloride functional group and a phenylmethylsulfonyl moiety. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its reactivity due to the presence of the acyl chloride functional group, which can readily participate in nucleophilic acyl substitution reactions. The sulfonyl group enhances its electrophilicity, making it a useful intermediate in organic synthesis, particularly in the preparation of sulfonamide derivatives and other complex molecules. The compound is likely to be sensitive to moisture and should be handled under anhydrous conditions to prevent hydrolysis. Safety precautions are essential, as it may be corrosive and can cause irritation upon contact with skin or mucous membranes. Proper storage in a cool, dry place away from incompatible substances is recommended to maintain its stability and reactivity.

Formula: C₁₁H₁₃ClO₃S

InChI: InChI=1S/C11H13ClO3S/c12-11(13)7-4-8-16(14,15)9-10-5-2-1-3-6-10/h1-3,5-6H,4,7-9H2

InChI key: InChIKey=HSDRPCACMINOQJ-UHFFFAOYSA-N

SMILES: C(S(CCCC(Cl)=O)(=O)=O)C1=CC=CC=C1

Synonyms:

• Butanoyl chloride, 4-[(phenylmethyl)sulfonyl]-
• 4-[(Phenylmethyl)sulfonyl]butanoyl chloride

4-Phenylmethanesulfonylbutanoyl chloride

CAS: 1706462-05-6

Versatile small molecule scaffold

Formula: C₁₁H₁₃ClO₃S

Purity: Min. 95%

Molecular weight: 260.74 g/mol

Ref: 3D-GTC46205