CAS 337508-66-4
:4-(1,3-oxazol-5-yl)benzenesulfonyl chloride
Description:
4-(1,3-Oxazol-5-yl)benzenesulfonyl chloride is an organic compound characterized by the presence of a sulfonyl chloride functional group attached to a benzene ring, which is further substituted with an oxazole ring. This compound typically appears as a solid or crystalline substance and is known for its reactivity due to the sulfonyl chloride moiety, which can participate in nucleophilic substitution reactions. The oxazole ring contributes to its heterocyclic nature, potentially influencing its biological activity and solubility properties. It is often used in organic synthesis, particularly in the preparation of sulfonamide derivatives and other functionalized compounds. The presence of both the aromatic and heterocyclic components may impart unique electronic properties, making it useful in various applications, including pharmaceuticals and agrochemicals. Safety precautions are necessary when handling this compound, as sulfonyl chlorides can be corrosive and may release toxic gases upon reaction with water or moisture.
Formula:C9H6ClNO3S
InChI:InChI=1/C9H6ClNO3S/c10-15(12,13)8-3-1-7(2-4-8)9-5-11-6-14-9/h1-6H
SMILES:c1cc(ccc1c1cnco1)S(=O)(=O)Cl
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 3 products.
4-(1,3-Oxazol-5-yl)benzenesulfonyl chloride
CAS:Formula:C9H6ClNO3SPurity:97%Color and Shape:SolidMolecular weight:243.66684-(1,3-Oxazol-5-yl)benzenesulphonyl chloride
CAS:<p>4-(1,3-Oxazol-5-yl)benzenesulphonyl chloride</p>Formula:C9H6ClNO3SPurity:≥95%Color and Shape: faint yellow to light orange solidMolecular weight:243.66684g/mol4-Oxazol-5-yl-benzenesulfonyl chloride
CAS:Formula:C9H6ClNO3SPurity:97%Color and Shape:Off-white solidMolecular weight:243.66


