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CAS 391248-15-0

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tert-butyl (4R)-4-cyano-1,3-thiazolidine-3-carboxylate

Description:
Tert-butyl (4R)-4-cyano-1,3-thiazolidine-3-carboxylate is a chemical compound characterized by its thiazolidine ring structure, which incorporates a cyano group and a tert-butyl ester functionality. This compound typically exhibits a white to off-white crystalline appearance and is soluble in organic solvents such as dichloromethane and ethanol, while being less soluble in water. The presence of the cyano group contributes to its reactivity, making it a potential intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. The thiazolidine moiety is known for its biological activity, often serving as a scaffold in medicinal chemistry. Additionally, the compound's chirality, indicated by the (4R) configuration, may influence its biological interactions and pharmacokinetics. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper laboratory practices are followed. Overall, tert-butyl (4R)-4-cyano-1,3-thiazolidine-3-carboxylate is a versatile compound with applications in various fields of chemistry.
Formula:C9H14N2O2S
InChI:InChI=1/C9H14N2O2S/c1-9(2,3)13-8(12)11-6-14-5-7(11)4-10/h7H,5-6H2,1-3H3/t7-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CSC[C@H]1C#N
Synonyms:
  • 3-Thiazolidinecarboxylic acid, 4-cyano-, 1,1-dimethylethyl ester, (4R)-
  • tert-Butyl (4R)-4-cyano-1,3-thiazolidine-3-carboxylate
  • tert-Butyl(R)-4-cyanothiazolidine-3-carboxylate
  • 4-cyano-3-thiazolidinecarboxylic acid
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