(R)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)propanoic acid

98%

  • Product Code: 39548
  Alias:    H-D-His(Trt)-OH
  CAS:    199119-46-5
Molecular Weight: 397.47 g./mol Molecular Formula: C₂₅H₂₃N₃O₂
EC Number: MDL Number:
Melting Point: Boiling Point: 584.8±50.0 °C
Density: 1.19 Storage Condition: 2-8 °C
Product Description: This chemical is primarily utilized in the field of medicinal chemistry and biochemistry as a key intermediate in the synthesis of complex molecules. It plays a significant role in the development of enzyme inhibitors and receptor modulators, particularly those targeting imidazole-related biological pathways. Its trityl-protected imidazole group makes it a valuable building block for peptide synthesis, enabling the creation of structurally diverse compounds with potential therapeutic applications. Researchers often employ it in the study of histidine-containing peptides and proteins, as well as in the design of novel drugs for treating conditions such as inflammation, cancer, and neurological disorders. Its chiral nature also allows for the exploration of stereospecific interactions in drug design, enhancing the precision of pharmacological agents.
Product Specification:
Test Specification
PURITY 97.5-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿2,700.00
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5.000 10-20 days ฿9,000.00
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(R)-2-Amino-3-(1-trityl-1H-imidazol-4-yl)propanoic acid
This chemical is primarily utilized in the field of medicinal chemistry and biochemistry as a key intermediate in the synthesis of complex molecules. It plays a significant role in the development of enzyme inhibitors and receptor modulators, particularly those targeting imidazole-related biological pathways. Its trityl-protected imidazole group makes it a valuable building block for peptide synthesis, enabling the creation of structurally diverse compounds with potential therapeutic applications. Researchers often employ it in the study of histidine-containing peptides and proteins, as well as in the design of novel drugs for treating conditions such as inflammation, cancer, and neurological disorders. Its chiral nature also allows for the exploration of stereospecific interactions in drug design, enhancing the precision of pharmacological agents.
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