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CS-W001157 4
Total: USD 88.00

tert-Butyl (R)-3-methyl-4-oxopiperidine-1-carboxylate

  • CAS No. 2091951-57-2

  • Cat. No. CS-0493278
  • Purity≥98%
  • MDL No.MFCD30342498

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

tert-Butyl (R)-3-methyl-4-oxopiperidine-1-carboxylate|CS-0493278

Structure of 2091951-57-2

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General Information

  • CAS No. 2091951-57-2
  • Cat. No. CS-0493278
  • Purity ≥98%
  • MDL No. MFCD30342498
  • Storage Store at room temperature
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₁₁H₁₉NO₃
  • Molecular Weight 213.27
  • Synonym(s) None
  • SMILES O=C1[C@H](C)CN(CC1)C(=O)OC(C)(C)C

Description

tert-Butyl (R)-3-methyl-4-oxopiperidine-1-carboxylate features a chiral piperidine core with a stereodefined methyl group and a ketone at the 4-position, enabling selective functionalization in asymmetric synthesis. The tert-butyl carbamate handle ensures stability and ease of removal under mild acidic conditions. This scaffold serves as a key building block for bioactive alkaloids and pharmaceutical intermediates.

Application

tert-Butyl (R)-3-methyl-4-oxopiperidine-1-carboxylate serves as a versatile chiral building block for the synthesis of piperidine-based pharmaceuticals and bioactive molecules. The protected amine and ketone functionalities enable sequential functionalization, including reductive amination and nucleophilic addition, with excellent stereocontrol. Its bench-stable nature and compatibility with standard coupling reactions facilitate efficient route development in medicinal chemistry.

Safety Information

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GHS Pictogram :
GHS No : GHS07
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H315-H319-H335
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501

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Computational Chemistry Data

  • TPSA   46.61
  • LogP   1.8324
  • H_Acceptors   3
  • H_Donors   0
  • Rotatable_Bonds   0

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