5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-4-carboxylic acid
95%
- Product Code: 87565
CAS:
1250997-59-1
| Molecular Weight: | 267.28 g./mol | Molecular Formula: | C₁₂H₁₇N₃O₄ |
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| EC Number: | MDL Number: | MFCD14581116 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting therapeutic areas such as inflammation, cancer, and neurological disorders. Its structure, featuring a tetrahydroimidazopyridine core, makes it a valuable building block for the design of small molecule drugs. Researchers often employ it in the synthesis of peptide mimetics and heterocyclic compounds, where its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during complex multi-step reactions. Additionally, its carboxylic acid functionality allows for further derivatization, enabling the creation of diverse chemical libraries for drug discovery and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿4,437.00 |
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| 0.005 | 10-20 days | ฿7,578.00 |
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5-(tert-Butoxycarbonyl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-4-carboxylic acid
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those targeting therapeutic areas such as inflammation, cancer, and neurological disorders. Its structure, featuring a tetrahydroimidazopyridine core, makes it a valuable building block for the design of small molecule drugs. Researchers often employ it in the synthesis of peptide mimetics and heterocyclic compounds, where its tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during complex multi-step reactions. Additionally, its carboxylic acid functionality allows for further derivatization, enabling the creation of diverse chemical libraries for drug discovery and optimization.
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