(S)-3-Amino-piperidine-2-one hydrochloride

95%

  • Product Code: 113882
  Alias:    Related CAS numbers: 406216-02-2; 138377-80-7; (S)-3-aminopiperidin-2-one hydrochloride
  CAS:    34294-79-6
Molecular Weight: 114.15 g./mol Molecular Formula: C₅H₁₀N₂O
EC Number: MDL Number: MFCD09259964
Melting Point: 180 °C Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of various therapeutic agents. It serves as a key intermediate in the production of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in the development of protease inhibitors, which are essential in treatments for viral infections like HIV. Its versatility also extends to the synthesis of bioactive molecules used in cancer research, where it contributes to the creation of compounds that inhibit tumor growth.
Product Specification:
Test Specification
Purity (Titration With Agno3) 94.5-105.5
Specific Rotation [α]20/D(C=0.5, Chcl3) -12
Appearance White To Light Yellow Powder Or Solid Or Chunks
Infrared Spectrum Conforms To Structure
Proton Nmr Spectrum Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days €43.00
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0.500 10-20 days €155.39
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1.000 10-20 days €284.93
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5.000 10-20 days €1,056.60
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(S)-3-Amino-piperidine-2-one hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of various therapeutic agents. It serves as a key intermediate in the production of drugs targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. Its chiral structure makes it valuable in creating enantiomerically pure compounds, which are crucial for enhancing drug efficacy and reducing side effects. Additionally, it is employed in the development of protease inhibitors, which are essential in treatments for viral infections like HIV. Its versatility also extends to the synthesis of bioactive molecules used in cancer research, where it contributes to the creation of compounds that inhibit tumor growth.
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