4-(Trifluoromethoxy)benzyl Bromide丨CAS 50824-05-0

4-(Trifluoromethoxy)benzyl Bromide丨CAS 50824-05-0
Product Introduction:
Catalog No.: SS123051
CAS No.: 50824-05-0
Assay: 99% min
Product Name: 4-(Trifluoromethoxy)benzyl bromide
Molecular Formula: C8H6OBrF3
Molecular Weight: 255.03
Synonym(s): 4-Trifluoromethoxybenzyl bromide
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Technical Parameters
Description

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Specifications

 

Item Specification
Appearance Light yellow liquid
Assay 99% min
Melting Point 22–24 °C
Moisture 0.5% max

 

Transport Information

 

Parameter

Specification

UN Number

3265

Class

8

Packing Group

II

H.S. Code

2909309090307

Stability & Reactivity

The product is chemically stable under standard ambient conditions.

Storage

Keep container tightly closed in a dry and well-ventilated place. Moisture sensitive.

Condition to Avoid

Avoid moisture.

Package

 

 

Manufacturing Information

 

Parameter

Specification

Capacity

 

Frequency

 

Main Export Countries

 

Capacity/Batch

 

Experience

Production since 2005

Stock

 

 

 

 

Applications

 

4-(Trifluoromethoxy)benzyl bromide (CAS 50824-05-0) is a halogenated aromatic compound widely used as an intermediate in pharmaceutical, agrochemical, and fine chemical synthesis. Its bromide functionality enables nucleophilic substitution reactions, making it useful for introducing the 4-(trifluoromethoxy)benzyl moiety into various target molecules. In medicinal chemistry, it is applied to synthesize bioactive compounds, including enzyme inhibitors, receptor ligands, and other drug candidates where the trifluoromethoxy group enhances metabolic stability and lipophilicity. It is also used in agrochemical research to prepare herbicides, fungicides, and insecticides with improved potency. Additionally, it serves as a building block for creating fluorinated aromatic derivatives in specialty chemicals and material sciences.

 

Benefits

 

The benefits of 4-(trifluoromethoxy)benzyl bromide stem from its reactive bromide and the presence of the trifluoromethoxy group. The bromide atom acts as a versatile leaving group, allowing selective substitution or cross-coupling reactions to generate a wide variety of functionalized molecules. The trifluoromethoxy group improves chemical and metabolic stability, increases lipophilicity, and can modulate electronic properties, enhancing bioactivity and pharmacokinetic profiles in medicinal compounds. Its combination of reactivity and fluorinated properties makes it a valuable intermediate for rapid and efficient synthesis of high-performance chemicals.

 

Conclusion

 

In summary, 4-(trifluoromethoxy)benzyl bromide is a multifunctional intermediate used in pharmaceuticals, agrochemicals, and fine chemical synthesis. Its applications include the preparation of bioactive molecules, fluorinated derivatives, and agrochemical agents, while its benefits lie in its reactive bromide, enhanced stability, and ability to improve lipophilicity and bioactivity. This compound remains a key building block for modern synthetic and medicinal chemistry.

 

 

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