CAS 1803567-40-9

2-Methyl-4-(trifluoromethyl)-5-thiazolemethanesulfonyl chloride

Description:

2-Methyl-4-(trifluoromethyl)-5-thiazolemethanesulfonyl chloride is a chemical compound characterized by its thiazole ring, which incorporates a methyl group and a trifluoromethyl group, enhancing its reactivity and potential applications in various chemical reactions. The presence of the sulfonyl chloride functional group indicates that it can act as a sulfonating agent, making it useful in organic synthesis, particularly in the preparation of sulfonamides and other derivatives. This compound is likely to be a solid at room temperature and may exhibit moderate to high stability under standard conditions, although it can be sensitive to moisture and should be handled with care due to the corrosive nature of the sulfonyl chloride group. Its unique structure may impart specific biological activities, making it of interest in pharmaceutical research. As with many specialized chemicals, safety precautions should be observed when handling, including the use of appropriate personal protective equipment and working in a well-ventilated area or fume hood.

Formula: C₆H₅ClF₃NO₂S₂

InChI: InChI=1S/C6H5ClF3NO2S2/c1-3-11-5(6(8,9)10)4(14-3)2-15(7,12)13/h2H2,1H3

InChI key: InChIKey=NLACIVCDBBHNKM-UHFFFAOYSA-N

SMILES: C(S(Cl)(=O)=O)C1=C(C(F)(F)F)N=C(C)S1

Synonyms:

• 2-Methyl-4-(trifluoromethyl)-5-thiazolemethanesulfonyl chloride
• 5-Thiazolemethanesulfonyl chloride, 2-methyl-4-(trifluoromethyl)-

[2-Methyl-4-(trifluoromethyl)-1,3-thiazol-5-yl]methanesulfonyl chloride

CAS: 1803567-40-9

Versatile small molecule scaffold

Formula: C₆H₅ClF₃NO₂S₂

Purity: Min. 95%

Molecular weight: 279.7 g/mol

Ref: 3D-DXC56740