4,6-Dibromo-3-fluoro-2-methylaniline
97%
- Product Code: 45951
CAS:
1000576-24-8
| Molecular Weight: | 282.9356 g./mol | Molecular Formula: | C₇H₆Br₂FN |
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| EC Number: | MDL Number: | MFCD09800762 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
4,6-Dibromo-3-fluoro-2-methylaniline is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. It serves as a key building block in the production of active pharmaceutical ingredients (APIs) and specialty chemicals. Its structure, featuring bromine and fluorine substituents, makes it valuable for creating molecules with specific biological activities, such as antimicrobial or antifungal agents. Additionally, it is utilized in the development of dyes and pigments due to its ability to introduce unique structural and electronic properties into the final product. Its role in chemical research also extends to the study of halogenated aromatic compounds, aiding in the exploration of new reactions and synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | €86.66 |
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4,6-Dibromo-3-fluoro-2-methylaniline
4,6-Dibromo-3-fluoro-2-methylaniline is primarily used as an intermediate in the synthesis of various organic compounds, particularly in the pharmaceutical and agrochemical industries. It serves as a key building block in the production of active pharmaceutical ingredients (APIs) and specialty chemicals. Its structure, featuring bromine and fluorine substituents, makes it valuable for creating molecules with specific biological activities, such as antimicrobial or antifungal agents. Additionally, it is utilized in the development of dyes and pigments due to its ability to introduce unique structural and electronic properties into the final product. Its role in chemical research also extends to the study of halogenated aromatic compounds, aiding in the exploration of new reactions and synthetic pathways.
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