(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-bromophenyl)butanoic acid
95%
- Product Code: 104244
CAS:
788149-96-2
| Molecular Weight: | 480.35 g./mol | Molecular Formula: | C₂₅H₂₂BrNO₄ |
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| EC Number: | MDL Number: | MFCD03788799 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key intermediate for constructing complex peptide chains. Its structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection during solid-phase peptide synthesis (SPPS), enabling precise control over the assembly of amino acids. The bromophenyl moiety enhances its reactivity in coupling reactions, making it valuable for introducing specific functionalities into peptides. Additionally, it is employed in the development of peptide-based pharmaceuticals, where its unique properties aid in the creation of targeted therapeutic agents. Its application extends to research in biochemistry and medicinal chemistry, particularly in the study of peptide interactions and drug design.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,445.00 |
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-bromophenyl)butanoic acid
This chemical is primarily utilized in the field of peptide synthesis, where it serves as a key intermediate for constructing complex peptide chains. Its structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for selective deprotection during solid-phase peptide synthesis (SPPS), enabling precise control over the assembly of amino acids. The bromophenyl moiety enhances its reactivity in coupling reactions, making it valuable for introducing specific functionalities into peptides. Additionally, it is employed in the development of peptide-based pharmaceuticals, where its unique properties aid in the creation of targeted therapeutic agents. Its application extends to research in biochemistry and medicinal chemistry, particularly in the study of peptide interactions and drug design.
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