3,4-Difluorobenzyl Bromide
98%
- Product Code: 117197
Alias:
3,4-difluorobenzyl bromide3,4-difluorobenzyl bromide3,4-difluorobenzyl bromide
CAS:
85118-01-0
| Molecular Weight: | 207.02 g./mol | Molecular Formula: | C₇H₅BrF₂ |
|---|---|---|---|
| EC Number: | 285-653-1 | MDL Number: | MFCD00009889 |
| Melting Point: | Boiling Point: | 59-61°C 3,5mm | |
| Density: | 1.618 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
3,4-Difluorobenzyl Bromide is widely used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a crucial role in the development of various bioactive molecules and drug candidates. Its structure, featuring both fluorine atoms and a reactive benzyl bromide group, makes it valuable for constructing complex chemical frameworks. It is often employed in coupling reactions, such as Suzuki or Heck reactions, to create aryl-alkyl bonds, which are essential in designing molecules with specific therapeutic properties. Additionally, it is utilized in the synthesis of agrochemicals and specialty chemicals, where its fluorinated aromatic ring contributes to enhanced stability and activity in the final products. The compound’s versatility also extends to material science, where it is used in the preparation of advanced polymers and coatings.
Product Specification:
| Test | Specification |
|---|---|
| Purity (HPLC) | 98-100 |
| Refractive Index N20/D | 1.524-1.527 |
| Specific Gravity (20/20 Degree Celsius) | 1.629-1.633 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿300.00 |
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| 5.000 | 10-20 days | ฿760.00 |
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| 25.000 | 10-20 days | ฿3,040.00 |
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3,4-Difluorobenzyl Bromide
3,4-Difluorobenzyl Bromide is widely used as a key intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a crucial role in the development of various bioactive molecules and drug candidates. Its structure, featuring both fluorine atoms and a reactive benzyl bromide group, makes it valuable for constructing complex chemical frameworks. It is often employed in coupling reactions, such as Suzuki or Heck reactions, to create aryl-alkyl bonds, which are essential in designing molecules with specific therapeutic properties. Additionally, it is utilized in the synthesis of agrochemicals and specialty chemicals, where its fluorinated aromatic ring contributes to enhanced stability and activity in the final products. The compound’s versatility also extends to material science, where it is used in the preparation of advanced polymers and coatings.
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