(R)-Piperidin-3-YlMethanol Hydrochloride

95%

  • Product Code: 37772
  CAS:    1124199-58-1
Molecular Weight: 151.63446 g./mol Molecular Formula: C₆H₁₄ClNO
EC Number: MDL Number: MFCD14155680
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: (R)-Piperidin-3-YlMethanol Hydrochloride finds its primary application in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. It is particularly significant in the development of drugs targeting the central nervous system, where its chiral structure plays a crucial role in enhancing the efficacy and selectivity of therapeutic agents. This compound is often utilized in the production of antipsychotic and antidepressant medications, contributing to the modulation of neurotransmitter systems. Additionally, it serves as a building block in the creation of ligands for receptor studies, aiding in the exploration of neurological pathways and drug discovery processes. Its versatility also extends to the synthesis of other pharmacologically active molecules, making it a valuable component in medicinal chemistry research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿639.00
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0.250 10-20 days ฿855.00
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1.000 10-20 days ฿3,357.00
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5.000 10-20 days ฿15,381.00
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(R)-Piperidin-3-YlMethanol Hydrochloride
(R)-Piperidin-3-YlMethanol Hydrochloride finds its primary application in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. It is particularly significant in the development of drugs targeting the central nervous system, where its chiral structure plays a crucial role in enhancing the efficacy and selectivity of therapeutic agents. This compound is often utilized in the production of antipsychotic and antidepressant medications, contributing to the modulation of neurotransmitter systems. Additionally, it serves as a building block in the creation of ligands for receptor studies, aiding in the exploration of neurological pathways and drug discovery processes. Its versatility also extends to the synthesis of other pharmacologically active molecules, making it a valuable component in medicinal chemistry research.
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