3-Bromo-2-fluorotoluene
98%
- Product Code: 117957
Alias:
3-Bromo-2-fluorotoluene
2-fluoro-3-bromotoluene
CAS:
59907-12-9
Molecular Weight: | 189.02 g./mol | Molecular Formula: | C₇H₆BrF |
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EC Number: | 261-981-0 | MDL Number: | MFCD04972694 |
Melting Point: | Boiling Point: | 186 °C | |
Density: | 1.52 | Storage Condition: | room temperature |
Product Description:
3-Bromo-2-fluorotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it a valuable building block for creating more complex molecules. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic rings with specific halogen functionalities into target compounds. This is crucial in drug discovery and development, where precise molecular modifications are required to optimize biological activity. Additionally, it is utilized in the synthesis of specialty chemicals, including dyes and electronic materials, where its halogenated aromatic system can contribute to desired properties like stability or reactivity. Its role in these applications highlights its importance in advancing industrial and medicinal chemistry.
Product Specification:
Test | Specification |
---|---|
Purity (GC) | 98-100 |
Refractive Index N20/D | 1.531-1.534 |
Specific Gravity (20/20) | 1.521-1.525 |
Appearance | Colorless To Light Yellow To Light Orange Clear Liquid |
Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿300.00 |
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5.000 | 10-20 days | ฿880.00 |
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3-Bromo-2-fluorotoluene
3-Bromo-2-fluorotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, featuring both bromine and fluorine substituents, makes it a valuable building block for creating more complex molecules. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic rings with specific halogen functionalities into target compounds. This is crucial in drug discovery and development, where precise molecular modifications are required to optimize biological activity. Additionally, it is utilized in the synthesis of specialty chemicals, including dyes and electronic materials, where its halogenated aromatic system can contribute to desired properties like stability or reactivity. Its role in these applications highlights its importance in advancing industrial and medicinal chemistry.
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