CAS 229956-98-3: 5-[5-(trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl chloride

Description: 5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl chloride is a chemical compound characterized by its unique structural features, which include a thiophene ring, an isoxazole moiety, and a sulfonyl chloride functional group. The presence of the trifluoromethyl group enhances its lipophilicity and may influence its reactivity and biological activity. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to act as a sulfonylating agent. The sulfonyl chloride group is reactive, allowing for the introduction of sulfonyl groups into various substrates. Additionally, the isoxazole ring contributes to the compound's potential as a bioactive molecule, as isoxazoles are often found in medicinal chemistry. The compound's properties, such as solubility and stability, can be influenced by the presence of the trifluoromethyl group and the sulfonyl chloride functionality. Overall, this compound represents a versatile intermediate in synthetic chemistry with potential applications in drug development.

Formula: C₈H₃ClF₃NO₃S₂

InChI: InChI=1/C8H3ClF3NO3S2/c9-18(14,15)7-2-1-5(17-7)4-3-6(16-13-4)8(10,11)12/h1-3H

5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl choride

CAS: 229956-98-3

• Color and Shape: Solid
• Molecular weight: 317.67999267578125

2-Thiophenesulfonyl chloride, 5-[5-(trifluoromethyl)-3-isoxazolyl]-

CAS: 229956-98-3

• Formula: C₈H₃ClF₃NO₃S₂
• Color and Shape: Solid
• Molecular weight: 317.6925

5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulphonyl chloride

CAS: 229956-98-3

• Formula: C₈H₃ClF₃NO₃S₂
• Purity: 97%
• Color and Shape: faint brown crystalline solid
• Molecular weight: 317.69g/mol

5-[5-(Trifluoromethyl)-1,2-Oxazol-3-Yl]-2-Thiophenesulfonyl

CAS: 229956-98-3

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• Formula: C₈H₃ClF₃NO₃S₂
• Purity: Min. 95%
• Molecular weight: 317.69 g/mol