S-N-Boc-Piperidine-2-carboxylic acid

98%

  • Product Code: 105685
  Alias:    (S)-N-Boc-2-Piperidine carboxylate (S)-1-Boc-piperidine-2-carboxylic acid (S)-(-)-1-(tert-butoxycarbonyl)-2-piperidinecarboxylic acid N-Boc-L-piperidine-2-carboxylic acid
  CAS:    26250-84-0
Molecular Weight: 229.27 g./mol Molecular Formula: C₁₁H₁₉NO₄
EC Number: MDL Number: MFCD00151904
Melting Point: 122-126 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: S-N-Boc-Piperidine-2-carboxylic acid is widely used in organic synthesis, particularly in the pharmaceutical industry, as a key intermediate for the preparation of various biologically active compounds. It serves as a building block in the synthesis of piperidine derivatives, which are essential in the development of drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease. Additionally, it is utilized in the production of peptidomimetics, which mimic the structure and function of peptides, aiding in the design of novel therapeutic agents. Its Boc-protected amine group allows for selective reactions, making it a valuable tool in multi-step synthetic processes.
Product Specification:
Test Specification
Appearance White To Off-White Powder
Purity (%) 97.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days €6.86
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1.000 10-20 days €9.50
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5.000 10-20 days €17.94
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25.000 10-20 days €68.07
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S-N-Boc-Piperidine-2-carboxylic acid
S-N-Boc-Piperidine-2-carboxylic acid is widely used in organic synthesis, particularly in the pharmaceutical industry, as a key intermediate for the preparation of various biologically active compounds. It serves as a building block in the synthesis of piperidine derivatives, which are essential in the development of drugs targeting neurological disorders, such as Alzheimer's disease and Parkinson's disease. Additionally, it is utilized in the production of peptidomimetics, which mimic the structure and function of peptides, aiding in the design of novel therapeutic agents. Its Boc-protected amine group allows for selective reactions, making it a valuable tool in multi-step synthetic processes.
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