(2S,4S)-4-(((Benzyloxy)carbonyl)amino)pyrrolidine-2-carboxylic acid

95%

  • Product Code: 36575
  CAS:    1279034-86-4
Molecular Weight: 264.2771 g./mol Molecular Formula: C₁₃H₁₆N₂O₄
EC Number: MDL Number: MFCD08704526
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This compound is primarily utilized in the field of peptide synthesis as a building block for creating complex peptide structures. Its chiral centers and functional groups make it valuable for designing peptides with specific stereochemistry and biological activity. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of protease inhibitors and other therapeutic agents targeting enzymatic pathways. Additionally, it serves as an intermediate in organic synthesis, enabling the construction of more complex molecules with potential applications in medicinal chemistry and drug discovery. Its benzyloxycarbonyl (Cbz) protecting group is particularly useful in peptide synthesis, as it can be selectively removed under mild conditions without affecting other sensitive functional groups.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿2,592.00
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(2S,4S)-4-(((Benzyloxy)carbonyl)amino)pyrrolidine-2-carboxylic acid
This compound is primarily utilized in the field of peptide synthesis as a building block for creating complex peptide structures. Its chiral centers and functional groups make it valuable for designing peptides with specific stereochemistry and biological activity. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of protease inhibitors and other therapeutic agents targeting enzymatic pathways. Additionally, it serves as an intermediate in organic synthesis, enabling the construction of more complex molecules with potential applications in medicinal chemistry and drug discovery. Its benzyloxycarbonyl (Cbz) protecting group is particularly useful in peptide synthesis, as it can be selectively removed under mild conditions without affecting other sensitive functional groups.
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