CAS 1955547-79-1

2-Thiophenesulfonyl chloride, 2-chlorotetrahydro-, 1,1-dioxide

Description:

2-Thiophenesulfonyl chloride, 2-chlorotetrahydro-, 1,1-dioxide is a chemical compound characterized by its sulfonyl chloride functional group attached to a thiophene ring. This compound typically exhibits properties associated with sulfonyl chlorides, such as being reactive towards nucleophiles, making it useful in various synthetic applications, particularly in organic chemistry. The presence of the thiophene ring contributes to its aromatic characteristics, which can influence its reactivity and stability. The compound is likely to be a solid at room temperature, with a distinct odor due to the presence of the sulfonyl chloride group. It is important to handle this substance with care, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or moisture. In terms of applications, it may be utilized in the synthesis of pharmaceuticals, agrochemicals, or as an intermediate in organic synthesis. Proper safety measures, including the use of personal protective equipment, are essential when working with this compound.

Formula: C₄H₆Cl₂O₄S₂

InChI: InChI=1S/C4H6Cl2O4S2/c5-4(12(6,9)10)2-1-3-11(4,7)8/h1-3H2

InChI key: InChIKey=VUWBNCANEPJBSH-UHFFFAOYSA-N

SMILES: S(Cl)(=O)(=O)C1(Cl)S(=O)(=O)CCC1

Synonyms:

• 2-Thiophenesulfonyl chloride, 2-chlorotetrahydro-, 1,1-dioxide

2-Chloro-1,1-dioxo-1λ⁶-thiolane-2-sulfonyl chloride

CAS: 1955547-79-1

Versatile small molecule scaffold

Formula: C₄H₆Cl₂O₄S₂

Purity: Min. 95%

Molecular weight: 253.1 g/mol

Ref: 3D-FDD54779