(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid
97%
- Product Code: 37431
CAS:
1481642-14-1
| Molecular Weight: | 383.40 g./mol | Molecular Formula: | C₂₁H₂₁NO₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23381239 | |
| Melting Point: | Boiling Point: | 625.3°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. The methoxy group on the pentanoic acid moiety provides additional stability and control during the synthesis process. Its application is crucial in the production of custom peptides for research, pharmaceuticals, and biotechnology, particularly in drug development and biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £56.79 |
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| 1.000 | 10-20 days | £113.99 |
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| 5.000 | 10-20 days | £331.59 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-methoxy-5-oxopentanoic acid
This chemical is primarily used in the field of peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amino functionality. This allows for selective deprotection during solid-phase peptide synthesis, enabling the stepwise assembly of peptide chains. The methoxy group on the pentanoic acid moiety provides additional stability and control during the synthesis process. Its application is crucial in the production of custom peptides for research, pharmaceuticals, and biotechnology, particularly in drug development and biochemical studies.
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