4-(tert-Butyl)picolinimidamide hydrochloride
≥95%
- Product Code: 126248
CAS:
949010-62-2
| Molecular Weight: | 213.71 g./mol | Molecular Formula: | C10H16ClN3 |
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| EC Number: | MDL Number: | MFCD12755575 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store in inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. It serves as a building block for the development of potential pharmaceutical agents, particularly in the creation of small molecule inhibitors targeting specific enzymes or receptors. Its structure is advantageous in drug discovery due to the presence of the picolinimidamide group, which can interact with biological targets through hydrogen bonding and other molecular interactions. Researchers often employ it in the design of compounds for treating diseases such as cancer, infectious diseases, or inflammatory conditions. Additionally, its tert-butyl group enhances the stability and bioavailability of the resulting drug candidates, making it a valuable component in optimizing drug-like properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $235.88 |
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4-(tert-Butyl)picolinimidamide hydrochloride
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. It serves as a building block for the development of potential pharmaceutical agents, particularly in the creation of small molecule inhibitors targeting specific enzymes or receptors. Its structure is advantageous in drug discovery due to the presence of the picolinimidamide group, which can interact with biological targets through hydrogen bonding and other molecular interactions. Researchers often employ it in the design of compounds for treating diseases such as cancer, infectious diseases, or inflammatory conditions. Additionally, its tert-butyl group enhances the stability and bioavailability of the resulting drug candidates, making it a valuable component in optimizing drug-like properties.
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