(9H-Fluoren-9-yl)methyl (3-aminopropyl)carbamate hydrochloride
95%
- Product Code: 121540
CAS:
210767-37-6
| Molecular Weight: | 332.82 g./mol | Molecular Formula: | C₁₈H₂₁CIN₂O₂ |
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| EC Number: | MDL Number: | MFCD00830742 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily used in the field of organic synthesis and peptide chemistry as a protecting group for amines. It is particularly effective in the protection of amino groups during the synthesis of peptides, preventing unwanted reactions and ensuring the desired sequence is achieved. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, can be easily removed under mild basic conditions, making it highly suitable for solid-phase peptide synthesis (SPPS). Additionally, it is employed in the preparation of various biologically active molecules and pharmaceuticals, where selective protection and deprotection of functional groups are crucial. Its stability and ease of removal make it a valuable tool in the development of complex organic compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft45,865.38 |
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(9H-Fluoren-9-yl)methyl (3-aminopropyl)carbamate hydrochloride
This compound is primarily used in the field of organic synthesis and peptide chemistry as a protecting group for amines. It is particularly effective in the protection of amino groups during the synthesis of peptides, preventing unwanted reactions and ensuring the desired sequence is achieved. The fluorenylmethyloxycarbonyl (Fmoc) group, which is part of this compound, can be easily removed under mild basic conditions, making it highly suitable for solid-phase peptide synthesis (SPPS). Additionally, it is employed in the preparation of various biologically active molecules and pharmaceuticals, where selective protection and deprotection of functional groups are crucial. Its stability and ease of removal make it a valuable tool in the development of complex organic compounds.
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