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Home  > 1-(Tetrahydro-pyran-4-yl)-1H-pyrazole-4-boronic acid pinacol ester

AB50587

1040377-03-4 | 1-(Tetrahydro-pyran-4-yl)-1H-pyrazole-4-boronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $5.00 $4.00 -   +
1g 98% in stock $10.00 $7.00 -   +
5g 98% in stock $37.00 $26.00 -   +
10g 98% in stock $74.00 $52.00 -   +
25g 98% in stock $175.00 $123.00 -   +
100g 98% in stock $699.00 $490.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB50587
Chemical Name: 1-(Tetrahydro-pyran-4-yl)-1H-pyrazole-4-boronic acid pinacol ester
CAS Number: 1040377-03-4
Molecular Formula: C14H23BN2O3
Molecular Weight: 278.155
MDL Number: MFCD12033229
SMILES: CC1(C)OB(OC1(C)C)c1cnn(c1)C1CCOCC1

 

Computed Properties
Complexity: 342  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 20  
Hydrogen Bond Acceptor Count: 4  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole, or $name$, is a versatile compound widely utilized in chemical synthesis. This unique molecule serves as a key building block in the creation of structurally complex organic compounds. Due to its specific chemical structure, $name$ is particularly valuable in the formation of novel heterocyclic compounds with diverse applications in medicinal chemistry, material science, and agrochemical research.In chemical synthesis, 1-(Tetrahydro-2H-pyran-4-yl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole acts as a valuable synthon, providing a convenient and efficient route for the introduction of both pyrazole and tetrahydropyran moieties into target molecules. The presence of boron within its structure further enhances its utility by enabling straightforward cross-coupling reactions to access a wide range of functionalized derivatives.By incorporating $name$ into synthetic pathways, chemists can access a diverse array of biologically active and structurally intricate compounds, making it an indispensable tool in the advancement of modern organic synthesis strategies.
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