(R)-(9H-Fluoren-9-yl)methyl (1-hydroxy-4-methylpentan-2-yl)carbamate
97%
- Product Code: 53051
CAS:
215178-41-9
Molecular Weight: | 339.43 g./mol | Molecular Formula: | C₂₁H₂₅NO₃ |
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EC Number: | MDL Number: | MFCD00270276 | |
Melting Point: | Boiling Point: | 525.204°C at 760 mmHg | |
Density: | 1.149g/cm3 | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protecting group for amino acids. The fluorenylmethyloxycarbonyl (Fmoc) group, a key component of this chemical, is widely employed to protect the amino group during the synthesis process. Its application ensures that the amino group remains unreactive while other functional groups undergo chemical reactions, allowing for the controlled assembly of peptide chains. After the synthesis, the Fmoc group can be easily removed under mild basic conditions, making it a valuable tool in solid-phase peptide synthesis (SPPS). This compound is particularly useful in the production of complex peptides and proteins for pharmaceutical and biochemical research.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,728.00 |
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0.250 | 10-20 days | ฿3,186.00 |
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1.000 | 10-20 days | ฿8,613.00 |
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(R)-(9H-Fluoren-9-yl)methyl (1-hydroxy-4-methylpentan-2-yl)carbamate
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protecting group for amino acids. The fluorenylmethyloxycarbonyl (Fmoc) group, a key component of this chemical, is widely employed to protect the amino group during the synthesis process. Its application ensures that the amino group remains unreactive while other functional groups undergo chemical reactions, allowing for the controlled assembly of peptide chains. After the synthesis, the Fmoc group can be easily removed under mild basic conditions, making it a valuable tool in solid-phase peptide synthesis (SPPS). This compound is particularly useful in the production of complex peptides and proteins for pharmaceutical and biochemical research.
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