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Atomfair Benzyl 2-hydroxypyrrolidine-1-carboxylate C12H15NO3

Description Benzyl 2-hydroxypyrrolidine-1-carboxylate (CAS No. 69261-54-7) is a high-purity organic compound with the molecular formula C12H15NO3. This white to off-white crystalline solid is a protected derivative of 2-hydroxypyrrolidine, featuring a benzyloxycarbonyl (Cbz) group, making it a valuable intermediate in peptide synthesis and medicinal chemistry. With a molecular weight of 221.25 g/mol, it is soluble in common organic solvents such as DCM, DMF, and methanol. Ideal for researchers in pharmaceutical development, this compound is rigorously tested for purity (typically ??95% by HPLC or GC) and is supplied with comprehensive analytical data, including1H NMR and LC-MS spectra. Store under inert conditions at…

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Description

Description

Benzyl 2-hydroxypyrrolidine-1-carboxylate (CAS No. 69261-54-7) is a high-purity organic compound with the molecular formula C12H15NO3. This white to off-white crystalline solid is a protected derivative of 2-hydroxypyrrolidine, featuring a benzyloxycarbonyl (Cbz) group, making it a valuable intermediate in peptide synthesis and medicinal chemistry. With a molecular weight of 221.25 g/mol, it is soluble in common organic solvents such as DCM, DMF, and methanol. Ideal for researchers in pharmaceutical development, this compound is rigorously tested for purity (typically ??95% by HPLC or GC) and is supplied with comprehensive analytical data, including 1H NMR and LC-MS spectra. Store under inert conditions at 2-8??C to ensure long-term stability.

  • CAS No: 69261-54-7
  • Molecular Formula: C12H15NO3
  • Molecular Weight: 221.25
  • Exact Mass: 221.10519334
  • Monoisotopic Mass: 221.10519334
  • IUPAC Name: benzyl 2-hydroxypyrrolidine-1-carboxylate
  • SMILES: C1CC(N(C1)C(=O)OCC2=CC=CC=C2)O
  • Synonyms: Benzyl 2-hydroxypyrrolidine-1-carboxylate, 69261-54-7, benzyl 2-hydroxy-1-pyrrolidinecarboxylate, 2-hydroxy-N-cbz-pyrrolidine, SCHEMBL3049973

Application

Benzyl 2-hydroxypyrrolidine-1-carboxylate is widely used as a key building block in the synthesis of bioactive molecules, particularly in the preparation of proline-based peptidomimetics. Its Cbz-protected hydroxyl group allows for selective deprotection in multi-step organic syntheses. This compound is also employed in the development of enzyme inhibitors and chiral catalysts due to its stereogenic center. Researchers utilize it in fragment-based drug discovery and as a precursor for heterocyclic scaffolds in medicinal chemistry.

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