trans-1-(tert-Butoxycarbonyl)-4-methylpiperidine-3-carboxylic acid
97%
- Product Code: 87826
CAS:
1271810-25-3
| Molecular Weight: | 243.3 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD27922261 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily used as an intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in organic synthesis, particularly in peptide chemistry. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations without unwanted side reactions. Additionally, the presence of the carboxylic acid group allows for further functionalization, such as amide bond formation, which is crucial in the development of active pharmaceutical ingredients (APIs). Its application is particularly relevant in the production of drugs targeting neurological and cardiovascular systems, where piperidine derivatives are commonly utilized.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £508.88 |
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trans-1-(tert-Butoxycarbonyl)-4-methylpiperidine-3-carboxylic acid
This chemical is primarily used as an intermediate in the synthesis of various pharmaceutical compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid moiety, makes it valuable in organic synthesis, particularly in peptide chemistry. The Boc group is often employed to protect amines during multi-step reactions, ensuring selective transformations without unwanted side reactions. Additionally, the presence of the carboxylic acid group allows for further functionalization, such as amide bond formation, which is crucial in the development of active pharmaceutical ingredients (APIs). Its application is particularly relevant in the production of drugs targeting neurological and cardiovascular systems, where piperidine derivatives are commonly utilized.
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