(2-(methylamino)pyridin-3-yl)methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate
98%
- Product Code: 36330
CAS:
1180002-01-0
| Molecular Weight: | 309.36 g./mol | Molecular Formula: | C₁₅H₂₃N₃O₄ |
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| EC Number: | MDL Number: | ||
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in the field of medicinal chemistry and pharmaceutical research. It serves as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring both a pyridine ring and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable for constructing compounds with potential activity as enzyme inhibitors or receptor modulators. Researchers often utilize it in the development of drugs that interact with neurotransmitter systems, such as dopamine or serotonin receptors, due to its ability to mimic certain pharmacophores. Additionally, its Boc-protected group allows for selective deprotection, enabling precise control during multi-step synthetic processes. This compound is also explored in the design of prodrugs, where its ester functionality can be hydrolyzed in vivo to release active drug molecules.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £10.40 |
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| 1.000 | 10-20 days | £26.69 |
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| 5.000 | 10-20 days | £81.87 |
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| 25.000 | 10-20 days | £275.93 |
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(2-(methylamino)pyridin-3-yl)methyl 2-((tert-butoxycarbonyl)(methyl)amino)acetate
This chemical is primarily used in the field of medicinal chemistry and pharmaceutical research. It serves as an intermediate in the synthesis of more complex molecules, particularly those targeting neurological and psychiatric disorders. Its structure, featuring both a pyridine ring and a tert-butoxycarbonyl (Boc) protected amine, makes it valuable for constructing compounds with potential activity as enzyme inhibitors or receptor modulators. Researchers often utilize it in the development of drugs that interact with neurotransmitter systems, such as dopamine or serotonin receptors, due to its ability to mimic certain pharmacophores. Additionally, its Boc-protected group allows for selective deprotection, enabling precise control during multi-step synthetic processes. This compound is also explored in the design of prodrugs, where its ester functionality can be hydrolyzed in vivo to release active drug molecules.
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