(S)-N-FMOC-4-Thiazoylalanine
98%
- Product Code: 57176
CAS:
205528-32-1
Molecular Weight: | 394.44 g./mol | Molecular Formula: | C₂₁H₁₈N₂O₄S |
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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 |
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APPEARANCE | White to Off-White Powder |
PURITY | 98-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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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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