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AB46513

99768-12-4 | 4-Methoxycarbonylphenylboronic acid

Packsize Purity Availability Price Discounted Price    Quantity
2g 98% in stock $6.00 $4.00 -   +
5g 98% in stock $9.00 $6.00 -   +
10g 98% in stock $12.00 $8.00 -   +
25g 98% in stock $23.00 $16.00 -   +
100g 98% in stock $79.00 $55.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB46513
Chemical Name: 4-Methoxycarbonylphenylboronic acid
CAS Number: 99768-12-4
Molecular Formula: C8H9BO4
Molecular Weight: 179.9657
MDL Number: MFCD01632203
SMILES: COC(=O)c1ccc(cc1)B(O)O

 

Computed Properties
Complexity: 175  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 4  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • Methyl 4-Boronobenzoate, a versatile compound widely used in chemical synthesis, serves as a crucial building block for the creation of various organic compounds. With its unique structure and reactivity, this compound plays a significant role in the development of pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, Methyl 4-Boronobenzoate can undergo various reactions such as cross-coupling reactions, Suzuki-Miyaura coupling, and Grignard reactions to form complex organic molecules. Its boron functionality enables efficient transformations, allowing for the introduction of aromatic groups, heteroatoms, and other functional groups to create diverse chemical structures.Furthermore, Methyl 4-Boronobenzoate's compatibility with a wide range of other reagents and catalysts makes it a valuable tool for the synthesis of challenging molecules with high precision and selectivity. Its utilization in the construction of key intermediates and active pharmaceutical ingredients highlights its importance in modern synthetic chemistry.Overall, Methyl 4-Boronobenzoate's versatility and reactivity make it an indispensable component in the toolbox of synthetic chemists, enabling the efficient assembly of complex organic molecules for various applications in the field of chemistry.
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