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CAS 62522-63-8

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3-Methyl-2-oxo-2,3-dihydrobenzo[d]oxazole-6-sulfonyl chloride

Description:
3-Methyl-2-oxo-2,3-dihydrobenzo[d]oxazole-6-sulfonyl chloride, with the CAS number 62522-63-8, is a chemical compound characterized by its unique structure, which includes a benzo[d]oxazole ring fused with a sulfonyl chloride functional group. This compound typically appears as a solid and is known for its reactivity due to the presence of the sulfonyl chloride moiety, which can participate in nucleophilic substitution reactions. The oxazole ring contributes to its potential biological activity, making it of interest in medicinal chemistry. The methyl group at the 3-position of the oxazole ring can influence the compound's solubility and reactivity. Additionally, the sulfonyl chloride group is a versatile electrophile, allowing for further derivatization and functionalization in synthetic applications. Overall, this compound's characteristics make it valuable in various chemical syntheses and potentially in pharmaceutical development. However, handling should be done with care due to the reactive nature of the sulfonyl chloride group.
Formula:C8H6ClNO4S
InChI:InChI=1S/C8H6ClNO4S/c1-10-6-3-2-5(15(9,12)13)4-7(6)14-8(10)11/h2-4H,1H3
InChI key:InChIKey=MRSCMVKREGBNOW-UHFFFAOYSA-N
SMILES:CN1C=2C(=CC(S(Cl)(=O)=O)=CC2)OC1=O
Synonyms:
  • 3-Methylbenzoxazolone-6-sulfonyl chloride
  • 2,3-Dihydro-3-methyl-2-oxo-6-benzoxazolesulfonyl chloride
  • 3-Methyl-2-oxo-2,3-dihydrobenzo[d]oxazole-6-sulfonyl chloride
  • 3-Methyl-2-oxo-2,3-dihydro-1,3-benzoxazole-6-sulfonyl chloride
  • 6-Benzoxazolesulfonyl chloride, 2,3-dihydro-3-methyl-2-oxo-
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