(9H-Fluoren-9-yl)methanamine hydrochloride
96%
- Product Code: 37156
CAS:
34221-61-9
| Molecular Weight: | 231.7207 g./mol | Molecular Formula: | C₁₄H₁₄ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06804511 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Used primarily in organic synthesis, it serves as a key reagent in the preparation of fluorenylmethyloxycarbonyl (Fmoc) protected amino acids, which are essential in peptide synthesis. This compound is widely applied in solid-phase peptide synthesis (SPPS) to protect amino groups during the assembly of peptide chains, ensuring selective deprotection and efficient coupling reactions. It is also utilized in the development of pharmaceuticals, particularly in the production of peptide-based drugs. Additionally, it finds use in biochemical research for labeling and modifying biomolecules, aiding in the study of protein interactions and functions. Its stability and ease of removal under mild conditions make it a preferred choice in these applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,292.00 |
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(9H-Fluoren-9-yl)methanamine hydrochloride
Used primarily in organic synthesis, it serves as a key reagent in the preparation of fluorenylmethyloxycarbonyl (Fmoc) protected amino acids, which are essential in peptide synthesis. This compound is widely applied in solid-phase peptide synthesis (SPPS) to protect amino groups during the assembly of peptide chains, ensuring selective deprotection and efficient coupling reactions. It is also utilized in the development of pharmaceuticals, particularly in the production of peptide-based drugs. Additionally, it finds use in biochemical research for labeling and modifying biomolecules, aiding in the study of protein interactions and functions. Its stability and ease of removal under mild conditions make it a preferred choice in these applications.
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