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Home  > Chemistry  > Heterocyclic Building Blocks  > Tetrahydropyrans  > 1-(Tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

AE11027

1082525-64-1 | 1-(Tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $25.00 $17.00 -   +
1g 95% in stock $80.00 $56.00 -   +
5g 95% in stock $360.00 $252.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE11027
Chemical Name: 1-(Tetrahydro-2H-pyran-2-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole
CAS Number: 1082525-64-1
Molecular Formula: C18H25BN2O3
Molecular Weight: 328.2137
MDL Number: MFCD12922967
SMILES: CC1(C)OB(OC1(C)C)c1ccc2c(c1)cnn2C1CCCCO1

 

Computed Properties
Complexity: 457  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 24  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 1  

 

 

Upstream Synthesis Route
  • In chemical synthesis, 1-(Tetrahydro-2H-pyran-2-yl)-1H-indazole-5-boronic acid pinacol ester serves as a versatile building block due to its unique structure and reactivity. This compound is commonly employed in the construction of complex organic molecules through Suzuki-Miyaura cross-coupling reactions. By utilizing its boronic acid functionality, it can selectively react with various aryl or vinyl halides under mild conditions, enabling the efficient formation of new carbon-carbon bonds. The presence of the pinacol ester moiety enhances the stability and solubility of the compound, making it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and functional materials.
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