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Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 5-Formylpyridine-2-boronic acid, hydrate

AA53910

1217500-70-3 | 5-Formylpyridine-2-boronic acid, hydrate

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $209.00 $147.00 -   +
250mg 95% in stock $401.00 $281.00 -   +
1g 95% in stock $867.00 $607.00 -   +

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*All prices are in USD.

Description
Catalog Number: AA53910
Chemical Name: 5-Formylpyridine-2-boronic acid, hydrate
CAS Number: 1217500-70-3
Molecular Formula: C6H8BNO4
Molecular Weight: 168.943
MDL Number: MFCD08703261
SMILES: OC(c1ccc(nc1)B(O)O)O

 

Computed Properties
Complexity: 142  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 5  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • (5-Formylpyridin-2-yl)boronic acid hydrate is a versatile chemical reagent widely used in chemical synthesis due to its unique properties and functions. As a boronic acid derivative, it plays a crucial role in Suzuki-Miyaura cross-coupling reactions, which are fundamental in the field of organic chemistry for forming carbon-carbon bonds. One key application of (5-Formylpyridin-2-yl)boronic acid hydrate is in the synthesis of biologically active compounds, pharmaceuticals, and functional materials. Its ability to efficiently undergo cross-coupling reactions with various aryl halides or triflates enables the construction of complex molecular structures with high efficiency and selectivity.In addition, (5-Formylpyridin-2-yl)boronic acid hydrate can also be utilized in the preparation of ligands for transition metal-catalyzed reactions, such as palladium-catalyzed C-C and C-N bond formations. This compound serves as a valuable building block in the design and synthesis of novel organic molecules with diverse applications in drug discovery, materials science, and agrochemicals.Overall, the application of (5-Formylpyridin-2-yl)boronic acid hydrate in chemical synthesis offers a powerful tool for organic chemists to access a wide range of structurally complex and biologically important compounds through efficient cross-coupling reactions and functional group transformations.
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