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CAS 196404-55-4

:

(4S,5R)-3-(tert-butoxycarbonyl)-2-(4-methoxyphenyl)-4-phenyl-1,3-oxazolidine-5-carboxylic acid

Description:
The chemical substance known as "(4S,5R)-3-(tert-butoxycarbonyl)-2-(4-methoxyphenyl)-4-phenyl-1,3-oxazolidine-5-carboxylic acid" with the CAS number 196404-55-4 is a chiral oxazolidine derivative. This compound features a bicyclic structure that includes an oxazolidine ring, which is characterized by the presence of both nitrogen and oxygen atoms in the ring. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amine functionality, enhancing the compound's stability and solubility. The presence of the 4-methoxyphenyl and phenyl substituents contributes to its aromatic character, potentially influencing its reactivity and interaction with biological systems. This compound may exhibit interesting pharmacological properties, making it relevant in medicinal chemistry, particularly in the development of antibiotics or other therapeutic agents. Its stereochemistry, indicated by the (4S,5R) configuration, is crucial for its biological activity, as the spatial arrangement of atoms can significantly affect how the molecule interacts with biological targets.
Formula:C22H25NO6
InChI:InChI=1/C22H25NO6/c1-22(2,3)29-21(26)23-17(14-8-6-5-7-9-14)18(20(24)25)28-19(23)15-10-12-16(27-4)13-11-15/h5-13,17-19H,1-4H3,(H,24,25)/t17-,18+,19?/m0/s1
Synonyms:
  • (4S,5R)-3-tert-butoxycarbony-2-(4-anisy)-4-phenyl-5-oxazolidinecarboxylic acid
  • (4S,5R)-3-tert-butoxycarbony-2-(4-anisyl)-4-phenyl-5-oxazolidinercarboxylicacid
  • (4S,5R)-3-tert-Butoxycarbony-2-(4-anisyl)-4-phenyl-5-oxazolidinecarboxylic acid
  • (2R,4S,5R)-3-(tert-Butoxycarbonyl)-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid
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