CAS 197719-27-0
:2,5-Dimethyl-1,3-oxazole-4-carbonyl chloride
Description:
2,5-Dimethyl-1,3-oxazole-4-carbonyl chloride is a chemical compound characterized by its oxazole ring structure, which features a five-membered heterocyclic framework containing both nitrogen and oxygen atoms. This compound is typically used in organic synthesis, particularly in the preparation of various pharmaceuticals and agrochemicals due to its reactive carbonyl chloride functional group. The presence of the carbonyl chloride moiety makes it a versatile intermediate for acylation reactions, allowing for the introduction of diverse functional groups. The dimethyl substitutions at the 2 and 5 positions of the oxazole ring contribute to its steric and electronic properties, influencing its reactivity and solubility. As with many carbonyl chlorides, it is important to handle this compound with care, as it can be reactive and may release hydrochloric acid upon hydrolysis. Overall, 2,5-Dimethyl-1,3-oxazole-4-carbonyl chloride is a valuable compound in synthetic organic chemistry, with applications that leverage its unique structural features.
Formula:C6H6ClNO2
InChI:InChI=1/C6H6ClNO2/c1-3-5(6(7)9)8-4(2)10-3/h1-2H3
SMILES:Cc1c(C(=O)Cl)nc(C)o1
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Found 2 products.
2,5-Dimethyl-1,3-oxazole-4-carbonyl chloride
CAS:<p>2,5-Dimethyl-1,3-oxazole-4-carbonyl chloride</p>Formula:C6H6ClNO2Purity:97%Color and Shape: off-white to pale brown crystalsMolecular weight:159.57g/mol

