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CAS 145588-94-9

:

(S)-4-BENZYL-1,3-OXAZOLIDINE-2-THIONE

Description:
(S)-4-Benzyl-1,3-oxazolidine-2-thione is a chiral compound characterized by its oxazolidine ring structure, which incorporates a thione functional group. This compound features a benzyl substituent at the 4-position of the oxazolidine ring, contributing to its stereochemical properties and potential biological activity. The thione group, which is a sulfur-containing functional group, can influence the compound's reactivity and interactions in various chemical environments. As a chiral molecule, it exists in two enantiomeric forms, with the (S)-configuration being of particular interest in pharmaceutical applications due to its potential selectivity in biological systems. The compound may exhibit properties such as solubility in organic solvents and stability under specific conditions, making it relevant in synthetic organic chemistry and medicinal chemistry. Its CAS number, 145588-94-9, allows for precise identification and retrieval of information regarding its properties, safety data, and applications in scientific literature and databases.
Formula:C10H11NOS
InChI:InChI=1/C10H11NOS/c13-10-11-9(7-12-10)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,11,13)/t9-/m0/s1
SMILES:c1ccc(cc1)C[C@H]1COC(=N1)S
Synonyms:
  • (S)-4-Benzyloxazolidine-2-Thione
  • 4-(S)-4-benzyl-1,3-oxazolidine-2-thione
  • 2-Oxazolidinethione,4-(phenylmethyl)-, (4S)-(
  • (S) -4- benzyl-oxazolidin-2-thione
  • (S)-4-Benzyloxazolidine-2-thione,99%e.e.
  • (S)-4-BENZYL-1,3-OXAZOLIDINE-2-THIONE
  • (S)-4-Benzyloxazolidine-2-thione >=97.0%
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