(S)-N-FMOC-4-Thiazoylalanine

98%

  • Product Code: 57176
  CAS:    205528-32-1
Molecular Weight: 394.44 g./mol Molecular Formula: C₂₁H₁₈N₂O₄S
EC Number: MDL Number: MFCD00672568
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, airtight
Product Description: (S)-N-FMOC-4-Thiazoylalanine is primarily utilized in the field of peptide synthesis. It serves as a crucial building block for the incorporation of thiazole-containing amino acids into peptides, which are often explored for their biological activities. The FMOC (9-fluorenylmethoxycarbonyl) group acts as a protective group for the amino function, ensuring selective reactions during peptide chain assembly. This compound is particularly valuable in the development of peptide-based pharmaceuticals, where the thiazole ring can enhance stability, bioavailability, and interaction with biological targets. Additionally, it is employed in research to study the structure-activity relationships of peptides, aiding in the design of novel therapeutic agents. Its application extends to the synthesis of peptide libraries for high-throughput screening in drug discovery.
Product Specification:
Test Specification
APPEARANCE White to Off-White Powder
PURITY 98-100
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days ฿1,998.00
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1.000 10-20 days ฿4,905.00
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5.000 10-20 days ฿17,865.00
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(S)-N-FMOC-4-Thiazoylalanine
(S)-N-FMOC-4-Thiazoylalanine is primarily utilized in the field of peptide synthesis. It serves as a crucial building block for the incorporation of thiazole-containing amino acids into peptides, which are often explored for their biological activities. The FMOC (9-fluorenylmethoxycarbonyl) group acts as a protective group for the amino function, ensuring selective reactions during peptide chain assembly. This compound is particularly valuable in the development of peptide-based pharmaceuticals, where the thiazole ring can enhance stability, bioavailability, and interaction with biological targets. Additionally, it is employed in research to study the structure-activity relationships of peptides, aiding in the design of novel therapeutic agents. Its application extends to the synthesis of peptide libraries for high-throughput screening in drug discovery.
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