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Home  > Chemistry  > Organic Building Blocks  > Trifluoromethyls  > 2-Formyl-4-(trifluoromethyl)phenylboronic acid

AA53949

1217501-35-3 | 2-Formyl-4-(trifluoromethyl)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $65.00 $45.00 -   +
250mg 98% in stock $73.00 $51.00 -   +
1g 98% in stock $126.00 $88.00 -   +
5g 98% in stock $440.00 $308.00 -   +
10g 98% in stock $758.00 $531.00 -   +
25g 98% in stock $1,504.00 $1,053.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA53949
Chemical Name: 2-Formyl-4-(trifluoromethyl)phenylboronic acid
CAS Number: 1217501-35-3
Molecular Formula: C8H6BF3O3
Molecular Weight: 217.9376
MDL Number: MFCD13195656
SMILES: O=Cc1cc(ccc1B(O)O)C(F)(F)F

 

Computed Properties
Complexity: 232  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 6  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • The (2-Formyl-4-(trifluoromethyl)phenyl)boronic acid is a versatile compound commonly used in chemical synthesis as a key building block. Its unique structure, featuring a boronic acid functional group and a trifluoromethylphenyl moiety, provides a wide range of applications in the synthesis of pharmaceuticals, agrochemicals, and materials.In organic synthesis, this compound is often employed as a reagent in Suzuki coupling reactions, where it serves as a coupling partner with aryl halides or pseudohalides to form biaryl compounds. This reaction is popular in the pharmaceutical industry for creating complex molecular structures efficiently.Furthermore, the boronic acid moiety in (2-Formyl-4-(trifluoromethyl)phenyl)boronic acid can undergo diverse transformations, such as Suzuki-Miyaura cross-coupling, Chan-Lam coupling, and Sonogashira reactions. These reactions enable the introduction of the trifluoromethylphenyl group into various organic molecules, enhancing their biological activity or physical properties.Overall, the (2-Formyl-4-(trifluoromethyl)phenyl)boronic acid plays a crucial role in modern organic synthesis as a valuable tool for constructing complex molecules with trifluoromethylphenyl functionalities, offering exciting opportunities for drug discovery and material science research.
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