2,5-Difluorobenzyl bromide
98%
- Product Code: 115389
Alias:
2,5-Difluorobenzyl bromide
2,5-Difluorobenzyl bromide
α-Bromo-2,5-difluorotoluene
CAS:
85117-99-3
| Molecular Weight: | 207.02 g./mol | Molecular Formula: | C₇H₅BrF₂ |
|---|---|---|---|
| EC Number: | 285-651-0 | MDL Number: | MFCD00009897 |
| Melting Point: | Boiling Point: | ||
| Density: | 1.609 g/mL at 25 °C(lit.) | Storage Condition: | room temperature, flammable area |
Product Description:
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive benzyl bromide group allows for efficient alkylation reactions, making it valuable in constructing complex molecules. Additionally, it is employed in the development of fluorine-containing compounds, which are often sought after for their enhanced stability and bioavailability in drug design. The difluoro substitution on the benzene ring further contributes to its utility in creating materials with specific electronic properties, useful in advanced material science applications.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98 |
| Refractive Index N20/D | 1.525-1.528 |
| Specific Gravity (20/20 Degree Celsius) | 1.632-1.638 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿340.00 |
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| 5.000 | 10-20 days | ฿430.00 |
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| 25.000 | 10-20 days | ฿1,900.00 |
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2,5-Difluorobenzyl bromide
Used primarily in organic synthesis, this compound serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive benzyl bromide group allows for efficient alkylation reactions, making it valuable in constructing complex molecules. Additionally, it is employed in the development of fluorine-containing compounds, which are often sought after for their enhanced stability and bioavailability in drug design. The difluoro substitution on the benzene ring further contributes to its utility in creating materials with specific electronic properties, useful in advanced material science applications.
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