(R)-4-((9H-fluoren-9-yl)methoxy)-2-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid
95%
- Product Code: 104275
CAS:
123417-19-6
| Molecular Weight: | 411.45 g./mol | Molecular Formula: | C₂₃H₂₅NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00151867 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a crucial building block for constructing complex peptide chains. Its structure is designed to protect amino groups during the synthesis process, ensuring that reactions occur at the desired sites without interference. The fluorenylmethyloxycarbonyl (Fmoc) group in its structure is particularly important, as it provides temporary protection for amino acids, which can be selectively removed under mild conditions. This allows for precise control over the peptide assembly process. Additionally, the tert-butoxycarbonyl (Boc) group offers further protection, enhancing the stability of the compound during synthesis. Its application is essential in producing peptides for pharmaceutical research, drug development, and biochemical studies, where high purity and specificity are critical.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,574.00 |
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| 0.250 | 10-20 days | ฿4,680.00 |
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| 1.000 | 10-20 days | ฿9,360.00 |
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(R)-4-((9H-fluoren-9-yl)methoxy)-2-((tert-butoxycarbonyl)amino)-4-oxobutanoic acid
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a crucial building block for constructing complex peptide chains. Its structure is designed to protect amino groups during the synthesis process, ensuring that reactions occur at the desired sites without interference. The fluorenylmethyloxycarbonyl (Fmoc) group in its structure is particularly important, as it provides temporary protection for amino acids, which can be selectively removed under mild conditions. This allows for precise control over the peptide assembly process. Additionally, the tert-butoxycarbonyl (Boc) group offers further protection, enhancing the stability of the compound during synthesis. Its application is essential in producing peptides for pharmaceutical research, drug development, and biochemical studies, where high purity and specificity are critical.
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