6-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)hexanoic acid
97%
- Product Code: 120390
CAS:
173690-47-6
| Molecular Weight: | 367.44 g./mol | Molecular Formula: | C₂₂H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30596881 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
Used primarily in peptide synthesis as a protecting group for amines, this compound ensures selective reactions by preventing unwanted interactions at the amine site. Its fluorenylmethyloxycarbonyl (Fmoc) group is particularly valued for its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis, where it helps in the stepwise construction of peptide chains. Additionally, its hexanoic acid moiety enhances solubility in organic solvents, facilitating smoother reactions and purification processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,421.00 |
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| 0.250 | 10-20 days | ฿4,842.00 |
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6-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)hexanoic acid
Used primarily in peptide synthesis as a protecting group for amines, this compound ensures selective reactions by preventing unwanted interactions at the amine site. Its fluorenylmethyloxycarbonyl (Fmoc) group is particularly valued for its stability under basic conditions and ease of removal under mild acidic conditions. This makes it highly effective in solid-phase peptide synthesis, where it helps in the stepwise construction of peptide chains. Additionally, its hexanoic acid moiety enhances solubility in organic solvents, facilitating smoother reactions and purification processes.
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