logo
Home  > Chemistry  > Organic Building Blocks  > Trifluoromethyls  > 5-Methoxy-2-(trifluoromethoxy)phenylboronic acid

AD67274

1079402-25-7 | 5-Methoxy-2-(trifluoromethoxy)phenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $249.00 $175.00 -   +
1g 97% in stock $556.00 $390.00 -   +
5g 97% in stock $1,878.00 $1,315.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AD67274
Chemical Name: 5-Methoxy-2-(trifluoromethoxy)phenylboronic acid
CAS Number: 1079402-25-7
Molecular Formula: C8H8BF3O4
Molecular Weight: 235.9529
MDL Number: MFCD12025981
SMILES: COc1ccc(c(c1)B(O)O)OC(F)(F)F

 

Computed Properties
Complexity: 224  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 7  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • The compound 5-Methoxy-2-(trifluoromethoxy)phenyl)boronic acid plays a crucial role in chemical synthesis as a versatile building block in organic reactions. With its boronic acid functionality, this compound can participate in Suzuki-Miyaura cross-coupling reactions, allowing for the efficient formation of carbon-carbon bonds. Additionally, its phenyl ring containing both methoxy and trifluoromethoxy substituents can serve as a directing group in C-H functionalization reactions, enabling selective modifications at specific positions within organic molecules. Overall, the diverse reactivity of 5-Methoxy-2-(trifluoromethoxy)phenyl)boronic acid makes it a valuable tool for the synthesis of complex organic compounds with tailored structures and properties.
FEATURED PRODUCTS