logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyridines  > 3-Picoline-4-boronic acid HCl

AB55063

1072952-40-9 | 3-Picoline-4-boronic acid HCl

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $203.00 $142.00 -   +
1g 97% in stock $480.00 $336.00 -   +
5g 97% in stock $1,412.00 $989.00 -   +
10g 97% in stock $2,345.00 $1,642.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB55063
Chemical Name: 3-Picoline-4-boronic acid HCl
CAS Number: 1072952-40-9
Molecular Formula: C6H9BClNO2
Molecular Weight: 173.4052
MDL Number: MFCD06659519
SMILES: OB(c1ccncc1C)O.Cl

 

Computed Properties
Complexity: 110  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 3-Methylpyridin-4-yl)boronic acid hydrochloride is a versatile chemical compound widely utilized in organic synthesis. Its primary application lies in the field of cross-coupling reactions, such as Suzuki-Miyaura coupling, where it serves as a valuable boronic acid derivative for the formation of carbon-carbon bonds.In the realm of chemical synthesis, this compound acts as a key building block for the construction of various functionalized molecules, including pharmaceuticals, agrochemicals, and materials. By enabling the selective introduction of the (3-Methylpyridin-4-yl) functional group into target molecules, it facilitates the creation of complex structures with enhanced properties and biological activities.Furthermore, the hydrochloride form of (3-Methylpyridin-4-yl)boronic acid offers improved stability and solubility, making it particularly advantageous for use in aqueous reaction conditions. Its compatibility with a wide range of substrates and transition metal catalysts underscores its significance as a valuable tool in the synthesis of diverse organic compounds.Overall, the application of (3-Methylpyridin-4-yl)boronic acid hydrochloride in chemical synthesis enables researchers to access new molecules and advance their understanding of structure-activity relationships, paving the way for the development of novel materials and therapeutics.
FEATURED PRODUCTS