cis-4-Azido-N-(tert-butoxycarbonyl)-L-proline

≥98%

  • Product Code: 76649
  CAS:    132622-65-2
Molecular Weight: 256.26 g./mol Molecular Formula: C₁₀H₁₆N₄O₄
EC Number: MDL Number: MFCD04115791
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in peptide synthesis and bioconjugation processes. It serves as a protected form of proline, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality, allowing selective reactions at other sites. The azido group enables click chemistry, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, which are widely employed in labeling, crosslinking, or modifying biomolecules. Its cis configuration can influence the conformational properties of peptides, making it valuable in designing bioactive compounds or studying protein structures. Additionally, it is utilized in the development of prodrugs, peptide-based therapeutics, and materials for drug delivery systems due to its compatibility with various organic transformations.
Product Specification:
Test Specification
APPEARANCE White to Almost white powder to crystal
PURITY 98-100
MELTING POINT 69.0-73.0
Infrared spectrum Conforms to Structure
Specific rotation a20DC1 Methanol -23.0
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.050 10-20 days ฿2,450.00
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cis-4-Azido-N-(tert-butoxycarbonyl)-L-proline
This chemical is primarily used in peptide synthesis and bioconjugation processes. It serves as a protected form of proline, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality, allowing selective reactions at other sites. The azido group enables click chemistry, particularly in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, which are widely employed in labeling, crosslinking, or modifying biomolecules. Its cis configuration can influence the conformational properties of peptides, making it valuable in designing bioactive compounds or studying protein structures. Additionally, it is utilized in the development of prodrugs, peptide-based therapeutics, and materials for drug delivery systems due to its compatibility with various organic transformations.
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