CAS 321309-40-4
:5-(1,3-oxazol-5-yl)-2-thiophenesulfonyl chloride
Description:
5-(1,3-Oxazol-5-yl)-2-thiophenesulfonyl chloride is a chemical compound characterized by its unique structural features, which include a thiophene ring and an oxazole moiety. 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 presence of the sulfonyl chloride functional group makes it a reactive electrophile, allowing it to participate in nucleophilic substitution reactions. The oxazole ring contributes to the compound's stability and can influence its reactivity and solubility. Additionally, the compound may exhibit specific physical properties such as a distinct melting point and solubility in organic solvents, which are important for its handling and application in laboratory settings. Safety precautions should be observed when working with this compound, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or moisture. Overall, this compound is significant in synthetic chemistry for its versatile reactivity and potential applications.
Formula:C7H4ClNO3S2
InChI:InChI=1/C7H4ClNO3S2/c8-14(10,11)7-2-1-6(13-7)5-3-9-4-12-5/h1-4H
SMILES:c1cc(sc1c1cnco1)S(=O)(=O)Cl
Synonyms:- 5-(1,3-Oxazol-5-Yl)Thiophene-2-Sulfonyl Chloride
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Found 3 products.
5-(1,3-Oxazol-5-yl)thiophene-2-sulphonyl chloride
CAS:<p>5-(1,3-Oxazol-5-yl)thiophene-2-sulphonyl chloride</p>Formula:C7H4ClNO3S2Purity:≥95%Color and Shape: orange solidMolecular weight:249.69g/mol5-(1,3-Oxazol-5-yl)thiophene-2-sulphonyl chloride
CAS:<p>Versatile small molecule scaffold</p>Formula:C7H4NO3S2ClPurity:Min. 95%Molecular weight:249.69 g/mol


