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AB56403

1072945-91-5 | 1-(2-Chlorophenyl)pyrazole-4-boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
250mg 96% in stock $291.00 $204.00 -   +
1g 96% in stock $884.00 $619.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB56403
Chemical Name: 1-(2-Chlorophenyl)pyrazole-4-boronic acid
CAS Number: 1072945-91-5
Molecular Formula: C9H8BClN2O2
Molecular Weight: 222.436
MDL Number: MFCD09972101
SMILES: Clc1ccccc1n1ncc(c1)B(O)O

 

Computed Properties
Complexity: 220  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 2  

 

 

Upstream Synthesis Route
  • 1-(2-Chlorophenyl)pyrazole-4-boronic acid is a versatile compound widely used in chemical synthesis. Its application lies predominantly in the field of organic chemistry, specifically in the realm of boronic acid chemistry. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 1-(2-Chlorophenyl)pyrazole-4-boronic acid acts as a crucial reagent for Suzuki-Miyaura cross-coupling reactions. This palladium-catalyzed coupling reaction allows for the formation of carbon-carbon bonds, enabling the assembly of complex molecular structures with high efficiency. By participating in such coupling reactions, this compound facilitates the creation of diverse organic molecules that are essential in the development of new drugs, crop protection agents, and functional materials.Additionally, 1-(2-Chlorophenyl)pyrazole-4-boronic acid can be utilized in the construction of heterocyclic compounds through various transformations, such as halogenation, arylation, and Suzuki coupling reactions. Its strategic placement of the boronic acid moiety enables selective functionalization at the pyrazole ring, offering synthetic chemists a valuable tool for designing and modifying molecular structures with precision.Overall, the versatile nature of 1-(2-Chlorophenyl)pyrazole-4-boronic acid makes it a valuable asset in the arsenal of organic chemists, enabling the efficient synthesis of diverse compounds with potential applications in pharmaceuticals, agrochemicals, and materials science.
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