(S)-3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan-

99%

  • Product Code: 50674
  Alias:    (S)-3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan-1-amine (S)-2-acetylaminopentanedioate
  CAS:    219921-94-5
Molecular Weight: 435.57 g./mol Molecular Formula: C₂₃H₃₇N₃O₅
EC Number: MDL Number: MFCD09840998
Melting Point: 168-171 °C Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: (S)-3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan- is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring a piperidine ring and a phenyl group, makes it a valuable building block for developing drugs targeting the central nervous system (CNS). It is particularly relevant in the creation of compounds with potential antipsychotic, antidepressant, or anxiolytic properties. Additionally, its chiral center allows for the development of enantiomerically pure drugs, which can enhance therapeutic efficacy and reduce side effects. Researchers also explore its use in designing ligands for receptor studies, aiding in the understanding of neurological pathways and drug-receptor interactions.
Product Specification:
Test Specification
Purity 98.5
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿460.00
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-
5.000 10-20 days ฿1,480.00
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25.000 10-20 days ฿5,000.00
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(S)-3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan-
(S)-3-Methyl-1-(2-(piperidin-1-yl)phenyl)butan- is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its structure, featuring a piperidine ring and a phenyl group, makes it a valuable building block for developing drugs targeting the central nervous system (CNS). It is particularly relevant in the creation of compounds with potential antipsychotic, antidepressant, or anxiolytic properties. Additionally, its chiral center allows for the development of enantiomerically pure drugs, which can enhance therapeutic efficacy and reduce side effects. Researchers also explore its use in designing ligands for receptor studies, aiding in the understanding of neurological pathways and drug-receptor interactions.
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