(S)-tert-butyl3-bromopiperidine-1-carboxylate
95%
- Product Code: 87186
CAS:
1354017-20-1
| Molecular Weight: | 264.16 g./mol | Molecular Formula: | C₁₀H₁₈BrNO₂ |
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| EC Number: | MDL Number: | MFCD19105582 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of various biologically active compounds. Its structure, featuring a bromine atom and a tert-butyloxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules, particularly in the development of piperidine-based drugs. It is often employed in the synthesis of potential therapeutic agents targeting neurological disorders, such as Alzheimer's disease and schizophrenia, due to its ability to modulate receptor activity. Additionally, it serves as a building block in the preparation of chiral compounds, enabling the creation of enantiomerically pure substances critical for drug efficacy and safety. Its reactivity and stability under various conditions make it a versatile tool in medicinal chemistry research.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿25,839.00 |
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| 1.000 | 10-20 days | ฿54,756.00 |
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(S)-tert-butyl3-bromopiperidine-1-carboxylate
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of various biologically active compounds. Its structure, featuring a bromine atom and a tert-butyloxycarbonyl (Boc) protecting group, makes it valuable for constructing complex molecules, particularly in the development of piperidine-based drugs. It is often employed in the synthesis of potential therapeutic agents targeting neurological disorders, such as Alzheimer's disease and schizophrenia, due to its ability to modulate receptor activity. Additionally, it serves as a building block in the preparation of chiral compounds, enabling the creation of enantiomerically pure substances critical for drug efficacy and safety. Its reactivity and stability under various conditions make it a versatile tool in medicinal chemistry research.
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