CAS 1339092-13-5

2-[(3-Methoxyphenyl)methoxy]ethanesulfonyl chloride

Description:

2-[(3-Methoxyphenyl)methoxy]ethanesulfonyl chloride, with the CAS number 1339092-13-5, is an organic compound characterized by the presence of a sulfonyl chloride functional group, which is known for its reactivity and ability to form sulfonamides. This compound features a methoxy-substituted phenyl group, contributing to its aromatic properties and potential for various chemical reactions. The sulfonyl chloride moiety makes it a useful intermediate in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. It is typically a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. The presence of the methoxy group enhances its solubility in organic solvents and may influence its reactivity. As with many sulfonyl chlorides, it is important to handle this compound with care due to its corrosive nature and potential to release hydrochloric acid upon reaction with water or alcohols. Proper safety measures, including the use of personal protective equipment, are essential when working with this substance in a laboratory setting.

Formula: C₁₀H₁₃ClO₄S

InChI: InChI=1S/C10H13ClO4S/c1-14-10-4-2-3-9(7-10)8-15-5-6-16(11,12)13/h2-4,7H,5-6,8H2,1H3

InChI key: InChIKey=YNKOZXHWJDGRRL-UHFFFAOYSA-N

SMILES: C(OCCS(Cl)(=O)=O)C1=CC(OC)=CC=C1

Synonyms:

• 2-[(3-Methoxyphenyl)methoxy]ethanesulfonyl chloride
• Ethanesulfonyl chloride, 2-[(3-methoxyphenyl)methoxy]-