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Home  > 2,3-Dichloro-4-methoxyphenylboronic acid

AA32283

1190219-72-7 | 2,3-Dichloro-4-methoxyphenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $273.00 $192.00 -   +
1g 98% in stock $556.00 $390.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA32283
Chemical Name: 2,3-Dichloro-4-methoxyphenylboronic acid
CAS Number: 1190219-72-7
Molecular Formula: C7H7BCl2O3
Molecular Weight: 220.8457
MDL Number: MFCD18384131
SMILES: COc1ccc(c(c1Cl)Cl)B(O)O

 

Computed Properties
Complexity: 170  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • (2,3-Dichloro-4-methoxyphenyl)boronic acid is a versatile compound commonly used in chemical synthesis as a key building block in various organic reactions. Its unique structure makes it a valuable reagent for cross-coupling reactions, especially in Suzuki-Miyaura coupling, which is a widely employed method for forming carbon-carbon bonds.This compound is highly effective in forming aryl-aryl, aryl-vinyl, and aryl-heteroatom bonds, making it a crucial component in the construction of complex organic molecules. Additionally, (2,3-Dichloro-4-methoxyphenyl)boronic acid exhibits excellent stability and compatibility with a wide range of functional groups, allowing for selective and efficient transformations in synthesis.Chemists rely on (2,3-Dichloro-4-methoxyphenyl)boronic acid for its reliable performance in facilitating key reactions that lead to the development of pharmaceuticals, agrochemicals, materials science, and other important chemical products. Its broad applicability and versatility make it a valuable tool for achieving precise and controlled bond formations in organic synthesis.
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