2,4-Dichloro-3-fluorobromobenzene
95%
- Product Code: 40774
CAS:
1000573-15-8
Molecular Weight: | 243.8885 g./mol | Molecular Formula: | C₆H₂BrCl₂F |
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EC Number: | MDL Number: | MFCD09878169 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
2,4-Dichloro-3-fluorobromobenzene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique halogen substitution pattern makes it a valuable building block for creating complex molecules. In pharmaceutical research, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into molecular structures. Additionally, it serves as a precursor in the synthesis of herbicides and pesticides, where its halogen atoms contribute to the bioactivity of the final compounds. The chemical is also utilized in material science for the preparation of specialty chemicals and advanced materials, leveraging its reactivity in cross-coupling reactions and other organic transformations.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿3,402.00 |
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2,4-Dichloro-3-fluorobromobenzene
2,4-Dichloro-3-fluorobromobenzene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique halogen substitution pattern makes it a valuable building block for creating complex molecules. In pharmaceutical research, it is often employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce specific functional groups into molecular structures. Additionally, it serves as a precursor in the synthesis of herbicides and pesticides, where its halogen atoms contribute to the bioactivity of the final compounds. The chemical is also utilized in material science for the preparation of specialty chemicals and advanced materials, leveraging its reactivity in cross-coupling reactions and other organic transformations.
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