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1-(tert-Butyl) 2-methyl (R)-4-oxopiperidine-1,2-dicarboxylate

  • CAS No. 1799811-83-8

  • Cat. No. CS-0132339
  • Purity≥95%
  • MDL No.MFCD12547038

*For research and further manufacturing use only, not for direct human use.

1-(tert-Butyl) 2-methyl (R)-4-oxopiperidine-1,2-dicarboxylate|CS-0132339

Structure of 1799811-83-8

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General Information

  • CAS No. 1799811-83-8
  • Cat. No. CS-0132339
  • Purity ≥95%
  • MDL No. MFCD12547038
  • Storage 4°C
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₂H₁₉NO₅
  • Molecular Weight None
  • Synonym(s) 1-tert-butyl 2-methyl (2R)-4-oxopiperidine-1,2-dicarboxylate
  • SMILES O=C(N1[C@@H](C(OC)=O)CC(CC1)=O)OC(C)(C)C

Description

This chiral piperidine derivative features a tert-butyl group at the nitrogen and a methyl substituent at the 2-position, delivering enhanced steric protection and stability. The (R)-configured scaffold integrates seamlessly into asymmetric synthesis workflows, enabling efficient access to complex alkaloid frameworks and bioactive molecules under standard conditions.

Application

1-(tert-Butyl) 2-methyl (R)-4-oxopiperidine-1,2-dicarboxylate serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to piperidine-containing scaffolds. Its tert-butyl ester group offers excellent bench stability and ease of removal under mild acidic conditions, while the methyl and oxo substituents provide defined stereochemistry and functional handles for downstream derivatization. The molecule facilitates stereoselective transformations in API synthesis and is compatible with standard coupling and reduction protocols.

Safety Information

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Computational Chemistry Data

  • TPSA   72.91
  • LogP   1.128
  • H_Acceptors   5
  • H_Donors   0
  • Rotatable_Bonds   1

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