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AA02341

1004294-79-4 | 3-Hydroxy-5-(methoxycarbonyl)phenylboronic acid, pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $102.00 $71.00 -   +
250mg 97% in stock $162.00 $113.00 -   +
1g 97% in stock $429.00 $300.00 -   +
5g 97% in stock $1,317.00 $922.00 -   +
10g 97% in stock $2,002.00 $1,402.00 -   +

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Description
Catalog Number: AA02341
Chemical Name: 3-Hydroxy-5-(methoxycarbonyl)phenylboronic acid, pinacol ester
CAS Number: 1004294-79-4
Molecular Formula: C14H19BO5
Molecular Weight: 278.1087
MDL Number: MFCD12546597
SMILES: COC(=O)c1cc(cc(c1)O)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 366  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route 
  • The compound Methyl 3-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate plays a crucial role in chemical synthesis as a reagent for Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool in organic chemistry for the creation of carbon-carbon bonds, commonly used in the assembly of complex organic molecules. By serving as a boronic ester, Methyl 3-hydroxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate enables the selective formation of aryl-aryl or aryl-vinyl bonds under mild reaction conditions. This versatile compound facilitates the construction of diverse chemical structures with high efficiency and selectivity, making it a valuable component in the toolkit of synthetic chemists.
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