6-Chloro-2-fluoro-3-methylbenzyl bromide
97%
- Product Code: 87645
CAS:
261762-88-3
| Molecular Weight: | 237.50 g./mol | Molecular Formula: | C₈H₇BrClF |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01631373 | |
| Melting Point: | 52-56 °C | Boiling Point: | |
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive benzyl bromide group makes it a valuable building block for constructing more complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). It is often employed in coupling reactions, such as Suzuki or Heck reactions, to introduce the benzyl moiety into target structures. Additionally, its chloro and fluoro substituents enhance its utility in creating compounds with specific electronic and steric properties, which are crucial for drug design and optimization. In agrochemical research, it serves as a precursor for synthesizing herbicides and pesticides, where the halogenated aromatic ring contributes to the desired biological activity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft9,599.73 |
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| 0.250 | 10-20 days | Ft32,483.94 |
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| 1.000 | 10-20 days | Ft89,209.61 |
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6-Chloro-2-fluoro-3-methylbenzyl bromide
This compound is primarily utilized in organic synthesis as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its reactive benzyl bromide group makes it a valuable building block for constructing more complex molecules, particularly in the development of active pharmaceutical ingredients (APIs). It is often employed in coupling reactions, such as Suzuki or Heck reactions, to introduce the benzyl moiety into target structures. Additionally, its chloro and fluoro substituents enhance its utility in creating compounds with specific electronic and steric properties, which are crucial for drug design and optimization. In agrochemical research, it serves as a precursor for synthesizing herbicides and pesticides, where the halogenated aromatic ring contributes to the desired biological activity.
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