Description

(R)-3-Benzyloxycarbonyl-4-oxazolidine carboxylic acid (CAS No. 97534-84-4) is a high-purity chiral oxazolidine derivative widely utilized in pharmaceutical research, organic synthesis, and asymmetric catalysis. With the molecular formula C₁₂H₁₃NO₅, this compound serves as a key intermediate in the synthesis of enantiomerically pure drugs, peptidomimetics, and bioactive molecules. Its benzyloxycarbonyl (Cbz) protecting group enhances stability while enabling selective deprotection under mild conditions. This product is rigorously characterized by NMR, HPLC, and mass spectrometry to ensure ≥98% chemical and optical purity, making it ideal for demanding applications in medicinal chemistry and academic research. Available in scalable quantities with customizable packaging to meet GMP and ISO standards.

Properties

• CAS Number: 97534-84-4
• Complexity: 314
• IUPAC Name: (4R)-3-benzyloxycarbonyloxazolidine-4-carboxylic acid
• InChI: InChI=1S/C12H13NO5/c14-11(15)10-7-17-8-13(10)12(16)18-6-9-4-2-1-3-5-9/h1-5,10H,6-8H2,(H,14,15)/t10-/m1/s1
• InChI Key: XRRRGBIMHQARMF-SNVBAGLBSA-N
• Exact Mass: 251.07937252
• Molecular Formula: C12H13NO5
• Molecular Weight: 251.23
• SMILES: C1[C@@H](N(CO1)C(=O)OCC2=CC=CC=C2)C(=O)O
• Topological: 76.1
• Monoisotopic Mass: 251.07937252
• Synonyms: 97534-84-4, (R)-3-Benzyloxycarbonyl-4-oxazolidine carboxylic acid, (R)-(+)-3-(Benzyloxycarbonyl)-4-oxazolidinecarboxylic acid, (R)-3-((Benzyloxy)carbonyl)oxazolidine-4-carboxylic acid, (4R)-3-phenylmethoxycarbonyl-1,3-oxazolidine-4-carboxylic acid, (R)-CBZ-OXAPROLINE, (4R)-3-[(BENZYLOXY)CARBONYL]-1,3-OXAZOLIDINE-4-CARBOXYLIC ACID, MFCD00274192, SCHEMBL3148090, DTXSID701215069, BS-42219, CS-0321599, F72117, (R)-3-((Benzyloxy)carbonyl)oxazolidine-4-carboxylicacid, (R)-(+)-3-Benzyloxycarbonyl-4-oxazolidinecarboxylic acid, 3,4-Oxazolidinedicarboxylicacid,3-(phenylmethyl)ester,(4R)-, (R)-(+)-3-(Benzyloxycarbonyl)-4-oxazolidinecarboxylic acid, 98%

This compound is primarily employed as a chiral building block for synthesizing β-amino acids and constrained peptides. It facilitates asymmetric transformations in organocatalysis and serves as a precursor for oxazolidinone-based pharmaceuticals. Researchers also use it to study enzyme inhibition and proteolytic stability in drug design.

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