4-Chloro-5-iodo-2,6-dimethylpyrimidine
97%
- Product Code: 47170
CAS:
83410-16-6
| Molecular Weight: | 268.4800 g./mol | Molecular Formula: | C₆H₆ClIN₂ |
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| EC Number: | MDL Number: | MFCD02081997 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex chemical structures. Its unique halogenated pyrimidine core makes it valuable in the synthesis of pharmaceutical intermediates, where it can serve as a precursor for the creation of active pharmaceutical ingredients (APIs). Additionally, it is often employed in the preparation of agrochemicals, contributing to the development of pesticides and herbicides. The presence of both chlorine and iodine atoms on the pyrimidine ring allows for further functionalization through various chemical reactions, such as cross-coupling reactions, which are essential in medicinal chemistry and materials science. Its application also extends to research settings, where it is used to study the reactivity and properties of halogenated heterocycles.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,763.00 |
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4-Chloro-5-iodo-2,6-dimethylpyrimidine
This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex chemical structures. Its unique halogenated pyrimidine core makes it valuable in the synthesis of pharmaceutical intermediates, where it can serve as a precursor for the creation of active pharmaceutical ingredients (APIs). Additionally, it is often employed in the preparation of agrochemicals, contributing to the development of pesticides and herbicides. The presence of both chlorine and iodine atoms on the pyrimidine ring allows for further functionalization through various chemical reactions, such as cross-coupling reactions, which are essential in medicinal chemistry and materials science. Its application also extends to research settings, where it is used to study the reactivity and properties of halogenated heterocycles.
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