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AA19752

114897-92-6 | 4-Bromo-2-fluorophenylacetic acid

Packsize Purity Availability Price Discounted Price    Quantity
10g 98% in stock $13.00 $10.00 -   +
25g 98% in stock $30.00 $21.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA19752
Chemical Name: 4-Bromo-2-fluorophenylacetic acid
CAS Number: 114897-92-6
Molecular Formula: C8H6BrFO2
Molecular Weight: 233.0344
MDL Number: MFCD09032952
SMILES: OC(=O)Cc1ccc(cc1F)Br

 

Computed Properties
Complexity: 174  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.2  

 

 

Upstream Synthesis Route
  • 2-(4-Bromo-2-fluorophenyl)acetic acid, also known as $name$, serves as a versatile building block in chemical synthesis. This compound is widely used in organic chemistry as a key intermediate for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its unique structure, characterized by the presence of bromine and fluorine substituents on the phenyl ring, confers specific reactivity that enables the formation of complex molecular structures.In chemical synthesis, 2-(4-Bromo-2-fluorophenyl)acetic acid can undergo a range of transformations, including nucleophilic substitution, organometallic reactions, and cross-coupling reactions. These reactions allow for the introduction of diverse functional groups and stereochemical elements into the final products. The bromine and fluorine atoms attached to the phenyl ring also provide handles for further derivatization, enhancing the compound's utility in the preparation of structurally diverse molecules.Additionally, the carboxylic acid functionality in 2-(4-Bromo-2-fluorophenyl)acetic acid serves as a versatile anchoring group for further modification through amidation, esterification, or condensation reactions. This feature enables the incorporation of this compound into more complex molecular scaffolds, expanding its synthetic potential in drug discovery and materials science.In summary, the strategic placement of bromine, fluorine, and carboxylic acid functionalities in 2-(4-Bromo-2-fluorophenyl)acetic acid makes it a valuable building block for chemical synthesis, offering a wide range of synthetic possibilities and applications in the development of novel compounds with diverse biological and chemical properties.
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