4,6-Dichloro-5-(4-bromophenyl)pyrimidine
99%
- Product Code: 48249
CAS:
146533-41-7
| Molecular Weight: | 303.97 g./mol | Molecular Formula: | C₁₀H₅BrCl₂N₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13151897 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both chloro and bromo substituents, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyrimidine moiety into target compounds. This is especially valuable in the synthesis of biologically active molecules, including potential drug candidates for treating various diseases. Additionally, its halogenated nature allows for further functionalization, enabling researchers to tailor its properties for specific applications in medicinal chemistry or material science.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 98.5 100% |
| Appearance | WHITE TO LIGHT YELLOW SOLID |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $16.80 |
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| 5.000 | 10-20 days | $58.21 |
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| 25.000 | 10-20 days | $209.72 |
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| 100.000 | 10-20 days | $734.17 |
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4,6-Dichloro-5-(4-bromophenyl)pyrimidine
This compound is primarily utilized in the field of organic synthesis, particularly as a key intermediate in the development of pharmaceuticals and agrochemicals. Its structure, featuring both chloro and bromo substituents, makes it a versatile building block for constructing more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce the pyrimidine moiety into target compounds. This is especially valuable in the synthesis of biologically active molecules, including potential drug candidates for treating various diseases. Additionally, its halogenated nature allows for further functionalization, enabling researchers to tailor its properties for specific applications in medicinal chemistry or material science.
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