tert-Butyl 3-(((benzyloxy)carbonyl)amino)pyrrolidine-1-carboxylate

97%

  • Product Code: 117354
  CAS:    325775-36-8
Molecular Weight: 320.38 g./mol Molecular Formula: C₁₇H₂₄N₂O₄
EC Number: MDL Number: MFCD11501516
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, sealed, dry
Product Description: This chemical is widely used in organic synthesis, particularly in the pharmaceutical industry, as a key intermediate in the production of various bioactive compounds. Its structure, featuring both tert-butyl and benzyloxycarbonyl protecting groups, makes it valuable in peptide synthesis and the development of protease inhibitors. It is often employed in the construction of complex molecules, where selective deprotection of these groups allows for controlled stepwise reactions. Additionally, it serves as a building block in the synthesis of pyrrolidine-based compounds, which are commonly found in drugs targeting central nervous system disorders, inflammation, and infectious diseases. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry research.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿9,018.00
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0.250 10-20 days ฿15,120.00
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1.000 10-20 days ฿37,800.00
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tert-Butyl 3-(((benzyloxy)carbonyl)amino)pyrrolidine-1-carboxylate
This chemical is widely used in organic synthesis, particularly in the pharmaceutical industry, as a key intermediate in the production of various bioactive compounds. Its structure, featuring both tert-butyl and benzyloxycarbonyl protecting groups, makes it valuable in peptide synthesis and the development of protease inhibitors. It is often employed in the construction of complex molecules, where selective deprotection of these groups allows for controlled stepwise reactions. Additionally, it serves as a building block in the synthesis of pyrrolidine-based compounds, which are commonly found in drugs targeting central nervous system disorders, inflammation, and infectious diseases. Its versatility and stability under various reaction conditions make it a preferred choice in medicinal chemistry research.
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