(S)-()-3-Piperidinecarboxylic acid

98%

  • Product Code: 60208
  CAS:    59045-82-8
Molecular Weight: 129.16 g./mol Molecular Formula: C₆H₁₁NO₂
EC Number: MDL Number: MFCD01630807
Melting Point: 254 °C (dec.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: (S)-()-3-Piperidinecarboxylic acid is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various drugs. It plays a crucial role in the development of compounds with therapeutic properties, particularly in the creation of chiral molecules that are essential for active pharmaceutical ingredients (APIs). Its structure is valuable in designing drugs targeting the central nervous system, including treatments for neurological disorders and pain management. Additionally, it is utilized in the production of alkaloids and other bioactive compounds, contributing to advancements in medicinal chemistry. Its enantiomeric purity makes it particularly useful in creating optically active substances, ensuring higher efficacy and specificity in drug formulations.
Product Specification:
Test Specification
ENANTIOMERIC EXCESS 98 100%
PURITYTITRATION BY HCLO4 98 103.5%
SPECIFIC ROTATION A20DC5 H2O 5-6
APPEARANCE White to tan solid
INFRARED SPECTRUM Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $37.57
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-
5.000 10-20 days $163.43
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(S)-()-3-Piperidinecarboxylic acid
(S)-()-3-Piperidinecarboxylic acid is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various drugs. It plays a crucial role in the development of compounds with therapeutic properties, particularly in the creation of chiral molecules that are essential for active pharmaceutical ingredients (APIs). Its structure is valuable in designing drugs targeting the central nervous system, including treatments for neurological disorders and pain management. Additionally, it is utilized in the production of alkaloids and other bioactive compounds, contributing to advancements in medicinal chemistry. Its enantiomeric purity makes it particularly useful in creating optically active substances, ensuring higher efficacy and specificity in drug formulations.
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