(9H-Fluoren-9-yl)methyl (5-aminopentyl)carbamate
98%
- Product Code: 192223
CAS:
118119-32-7
| Molecular Weight: | 324.42 g./mol | Molecular Formula: | C₂₀H₂₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01318871 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used primarily as a reagent in organic synthesis, especially in peptide and protein chemistry. It serves as a protecting group for amines due to its stability under various reaction conditions and selective removal under mild acidic conditions. Commonly employed in solid-phase peptide synthesis (SPPS), it helps prevent unwanted side reactions by masking amine functionalities. The fluorenylmethyl carbamate (Fmoc) group allows for stepwise assembly of peptides and is widely compatible with other functional groups, making it ideal for synthesizing complex biomolecules. Also used in the preparation of amino-functionalized polymers, linkers for bioconjugation, and in the development of pharmaceutical intermediates where controlled deprotection is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿6,110.00 |
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| 5.000 G | 10-20 days | ฿22,430.00 |
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(9H-Fluoren-9-yl)methyl (5-aminopentyl)carbamate
Used primarily as a reagent in organic synthesis, especially in peptide and protein chemistry. It serves as a protecting group for amines due to its stability under various reaction conditions and selective removal under mild acidic conditions. Commonly employed in solid-phase peptide synthesis (SPPS), it helps prevent unwanted side reactions by masking amine functionalities. The fluorenylmethyl carbamate (Fmoc) group allows for stepwise assembly of peptides and is widely compatible with other functional groups, making it ideal for synthesizing complex biomolecules. Also used in the preparation of amino-functionalized polymers, linkers for bioconjugation, and in the development of pharmaceutical intermediates where controlled deprotection is required.
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