(R)-1-Boc-3-Isopropylpiperazine

≥95%

  • Product Code: 113472
  CAS:    928025-63-2
Molecular Weight: 228.33 g./mol Molecular Formula: C₁₂H₂₄N₂O₂
EC Number: MDL Number: MFCD07772113
Melting Point: Boiling Point: 298.4°C at 760 mmHg
Density: Storage Condition: 2-8°C, protected from light, stored in an inert gas
Product Description: This compound is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the production of enantiomerically pure drugs, which are often more effective and have fewer side effects. It is commonly employed in the development of drugs targeting the central nervous system, including antidepressants and antipsychotics. Additionally, it serves as a building block in the creation of complex molecules for medicinal chemistry research, enabling the exploration of new therapeutic agents. Its Boc-protected amine group allows for selective deprotection, facilitating further chemical modifications in multi-step synthetic processes.
Product Specification:
Test Specification
Appearance Colorless To Light Yellow Liquid
Purity (%) 94.5-100
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿6,930.00
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1.000 10-20 days ฿16,320.00
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-
5.000 10-20 days ฿48,960.00
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-
10.000 10-20 days ฿96,280.00
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(R)-1-Boc-3-Isopropylpiperazine
This compound is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it particularly valuable in the production of enantiomerically pure drugs, which are often more effective and have fewer side effects. It is commonly employed in the development of drugs targeting the central nervous system, including antidepressants and antipsychotics. Additionally, it serves as a building block in the creation of complex molecules for medicinal chemistry research, enabling the exploration of new therapeutic agents. Its Boc-protected amine group allows for selective deprotection, facilitating further chemical modifications in multi-step synthetic processes.
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