5-Iodo-1,4-dimethyl-1H-1,2,3-triazole
≥95%
- Product Code: 49282
CAS:
1346818-62-9
| Molecular Weight: | 223.02 g./mol | Molecular Formula: | C₄H₆IN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28962625 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the construction of more complex molecules. Its unique structure, featuring both an iodine atom and a triazole ring, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the iodine atom allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researchers also explore its use in the development of fluorescent probes and imaging agents, leveraging the triazole moiety's ability to interact with biological systems. Its applications extend to material science, where it contributes to the synthesis of advanced polymers and coordination compounds with tailored properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $378.80 |
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| 0.250 | 10-20 days | $757.61 |
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5-Iodo-1,4-dimethyl-1H-1,2,3-triazole
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the construction of more complex molecules. Its unique structure, featuring both an iodine atom and a triazole ring, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the iodine atom allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researchers also explore its use in the development of fluorescent probes and imaging agents, leveraging the triazole moiety's ability to interact with biological systems. Its applications extend to material science, where it contributes to the synthesis of advanced polymers and coordination compounds with tailored properties.
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