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Home  > Chemistry  > Organic Building Blocks  > Trifluoromethyls  > 2-Bromo-4-fluoro-1-(trifluoromethyl)benzene

AB61377

351003-21-9 | 2-Bromo-4-fluoro-1-(trifluoromethyl)benzene

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $15.00 $10.00 -   +
1g 98% in stock $16.00 $11.00 -   +
5g 98% in stock $20.00 $14.00 -   +
10g 98% in stock $24.00 $17.00 -   +
25g 98% in stock $51.00 $36.00 -   +
100g 98% in stock $168.00 $117.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB61377
Chemical Name: 2-Bromo-4-fluoro-1-(trifluoromethyl)benzene
CAS Number: 351003-21-9
Molecular Formula: C7H3BrF4
Molecular Weight: 242.9963
MDL Number: MFCD03094041
SMILES: Fc1ccc(c(c1)Br)C(F)(F)F

 

Computed Properties
Complexity: 156  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 4  
XLogP3: 3.6  

 

 

Upstream Synthesis Route
  • 2-Bromo-4-fluorobenzotrifluoride is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. This compound is commonly employed as a key intermediate in the pharmaceutical and agrochemical industries, where it serves as a building block for the synthesis of various biologically active compounds.In organic synthesis, 2-Bromo-4-fluorobenzotrifluoride is frequently utilized for the introduction of a bromine atom into aromatic systems. This brominated benzene derivative can undergo a variety of reactions, such as nucleophilic aromatic substitution, transition metal-catalyzed cross-coupling reactions, and electrophilic aromatic substitution, allowing for the functionalization of the benzene ring at the 2 and 4 positions. Additionally, the trifluoromethyl group attached to the benzene ring enhances the compound's lipophilicity and metabolic stability, making it a valuable scaffold for drug design and discovery.Overall, 2-Bromo-4-fluorobenzotrifluoride plays a crucial role in the synthesis of complex molecules with medicinal and pesticidal properties, highlighting its significance in modern chemical research and development.
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