(9H-Fluoren-9-yl)methyl 3-aminopiperidine-1-carboxylate hydrochloride
97%
- Product Code: 37145
CAS:
811841-86-8
| Molecular Weight: | 358.8618 g./mol | Molecular Formula: | C₂₀H₂₃ClN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03001674 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological and psychiatric disorders. The fluorenylmethyl (Fmoc) group acts as a protecting group for amines during peptide synthesis, ensuring selective reactions and preventing unwanted side reactions. Its application extends to the synthesis of complex peptides and small molecules, where precise control over chemical reactions is crucial. Additionally, it is employed in the design of compounds for studying receptor interactions and enzyme inhibition, contributing to advancements in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $118.81 |
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(9H-Fluoren-9-yl)methyl 3-aminopiperidine-1-carboxylate hydrochloride
This compound is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of various biologically active molecules, particularly in the development of drugs targeting neurological and psychiatric disorders. The fluorenylmethyl (Fmoc) group acts as a protecting group for amines during peptide synthesis, ensuring selective reactions and preventing unwanted side reactions. Its application extends to the synthesis of complex peptides and small molecules, where precise control over chemical reactions is crucial. Additionally, it is employed in the design of compounds for studying receptor interactions and enzyme inhibition, contributing to advancements in medicinal chemistry.
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