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CAS 27685-90-1

:

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

Description:
2-Oxo-2,3-dihydrobenzo[d]oxazole-6-sulfonyl chloride, with the CAS number 27685-90-1, is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. This compound features a benzo[d]oxazole ring, which contributes to its aromatic properties and potential biological activity. The presence of the oxo group indicates that it has a carbonyl functionality, enhancing its electrophilic character. As a sulfonyl chloride, it can participate in nucleophilic substitution reactions, making it valuable in the synthesis of various derivatives, including sulfonamides and other sulfonyl-containing compounds. The compound is typically handled with care due to its reactivity, particularly with water and amines, which can lead to the release of hydrochloric acid. Its applications may extend to medicinal chemistry and materials science, where it can serve as an intermediate in the development of pharmaceuticals or functional materials. Proper safety measures should be observed when working with this compound due to its potential hazards.
Formula:C7H4ClNO4S
InChI:InChI=1/C7H4ClNO4S/c8-14(11,12)4-1-2-5-6(3-4)13-7(10)9-5/h1-3H,(H,9,10)
InChI key:InChIKey=IBHCNMJSVDRBSY-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C=1C=C2C(=CC1)NC(=O)O2
Synonyms:
  • 2,3-Dihydro-2-oxo-6-benzoxazolesulfonyl chloride
  • 2-Hydroxy-1,3-benzoxazole-6-sulfonyl chloride
  • 2-Oxo-2,3-Dihydro-1,3-Benzoxazole-6-Sulfonyl Chloride
  • 2-Oxo-2,3-dihydrobenzo[d]oxazole-6-sulfonyl chloride
  • 2-Oxo-2,3-dihydrobenzoxazole-6-sulfonyl chloride
  • 2-Oxo-3H-1,3-benzoxazole-6-sulfonyl chloride
  • 6-Benzoxazolesulfonyl chloride, 2,3-dihydro-2-oxo-
  • 6-Benzoxazolinesulfonyl chloride, 2-oxo-
  • Benzoxazalone, 6-sulfochloride
  • 2,3-Dihydro-2-oxobenzoxazole-6-sulphonyl chloride
  • See more synonyms
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