N-Boc-DL-pipecolinic acid

98%

  • Product Code: 58028
  Alias:    N-Boc-DL-piperidine-2-carboxylic acid (±)-1-tert-butoxycarbonyl-piperidine-2-carboxylic acid
  CAS:    98303-20-9
Molecular Weight: 229.27 g./mol Molecular Formula: C₁₁H₁₉NO₄
EC Number: MDL Number: MFCD0186287
Melting Point: 130-133 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: N-Boc-DL-pipecolinic acid is widely used in organic synthesis, particularly in the preparation of peptides and peptidomimetics. It serves as a key intermediate in the development of pharmaceuticals, where it is employed to introduce the pipecolinic acid moiety into drug molecules. This compound is also utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric synthesis. Additionally, it finds application in the production of bioactive compounds and natural product derivatives, contributing to the exploration of new therapeutic agents. Its Boc-protecting group ensures stability during synthetic processes, making it a valuable building block in medicinal chemistry and drug discovery.
Product Specification:
Test Specification
Purity 97.5 100%
Melting point 127 133?
APPEARANCE WHITE TO OFF-WHITE POWDER OR CRYSTALS
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿260.00
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5.000 10-20 days ฿350.00
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25.000 10-20 days ฿750.00
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-
100.000 10-20 days ฿2,850.00
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-
500.000 10-20 days ฿13,900.00
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N-Boc-DL-pipecolinic acid
N-Boc-DL-pipecolinic acid is widely used in organic synthesis, particularly in the preparation of peptides and peptidomimetics. It serves as a key intermediate in the development of pharmaceuticals, where it is employed to introduce the pipecolinic acid moiety into drug molecules. This compound is also utilized in the synthesis of chiral ligands and catalysts, which are essential in asymmetric synthesis. Additionally, it finds application in the production of bioactive compounds and natural product derivatives, contributing to the exploration of new therapeutic agents. Its Boc-protecting group ensures stability during synthetic processes, making it a valuable building block in medicinal chemistry and drug discovery.
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