logo
Home  > Chemistry  > Heterocyclic Building Blocks  > Pyrazoles  > 1-(2-Propen-1-yl)-1H-pyrazole-4-boronic acid pinacol ester

AA00928

1000801-78-4 | 1-(2-Propen-1-yl)-1H-pyrazole-4-boronic acid pinacol ester

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $50.00 $35.00 -   +
1g 97% in stock $100.00 $70.00 -   +
5g 97% in stock $372.00 $260.00 -   +
10g 97% in stock $581.00 $407.00 -   +
25g 97% in stock $1,226.00 $858.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA00928
Chemical Name: 1-(2-Propen-1-yl)-1H-pyrazole-4-boronic acid pinacol ester
CAS Number: 1000801-78-4
Molecular Formula: C12H19BN2O2
Molecular Weight: 234.1025
MDL Number: MFCD16659011
SMILES: C=CCn1ncc(c1)B1OC(C(O1)(C)C)(C)C

 

Computed Properties
Complexity: 291  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 17  
Hydrogen Bond Acceptor Count: 3  
Rotatable Bond Count: 3  

 

 

Upstream Synthesis Route
  • The compound 1-Allyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole is a versatile building block in chemical synthesis. It is commonly used as a key intermediate in the synthesis of various functionalized organic molecules. This compound enables the introduction of the allyl functional group into target molecules, providing a handle for further derivatization. Additionally, the boron-containing group in the molecule can undergo diverse transformations, such as Suzuki-Miyaura cross-coupling reactions, allowing for the incorporation of a wide range of substituents. Overall, 1-Allyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole plays a crucial role in the construction of complex organic compounds with tailored properties and functionalities.
FEATURED PRODUCTS