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AE12304

1092790-21-0 | Isoquinoline-7-boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 98% in stock $33.00 $23.00 -   +
250mg 98% in stock $53.00 $37.00 -   +
1g 98% in stock $126.00 $88.00 -   +
5g 98% in stock $438.00 $307.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AE12304
Chemical Name: Isoquinoline-7-boronic acid
CAS Number: 1092790-21-0
Molecular Formula: C9H8BNO2
Molecular Weight: 172.9763
MDL Number: MFCD08234617
SMILES: OB(c1ccc2c(c1)cncc2)O

 

Computed Properties
Complexity: 177  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 2  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • Isoquinolin-7-ylboronic acid is a valuable chemical reagent widely utilized in organic synthesis due to its versatility and reactivity. This compound serves as a crucial building block in the formation of various pharmacologically active molecules and functional materials.One prominent application of Isoquinolin-7-ylboronic acid is its role as a key intermediate in the Suzuki-Miyaura coupling reaction. This palladium-catalyzed cross-coupling reaction allows for the selective formation of carbon-carbon bonds between an aryl or vinyl boronic acid and an organic halide. By utilizing Isoquinolin-7-ylboronic acid in this reaction, chemists can efficiently construct complex molecular structures, such as biaryl compounds, which are essential in medicinal chemistry and material science.Additionally, Isoquinolin-7-ylboronic acid can participate in various other transformations, including transition metal-catalyzed cross-coupling reactions, oxidative coupling reactions, and C-H activation processes. Its unique structural features make it a valuable tool for introducing the Isoquinoline moiety into target molecules, enabling the synthesis of diverse heterocyclic compounds with potential biological activities.Overall, Isoquinolin-7-ylboronic acid plays a crucial role in modern organic synthesis, offering chemists the means to access structurally diverse compounds efficiently. Its significance in the development of pharmaceuticals, agrochemicals, and advanced materials highlights its importance in the field of synthetic chemistry.
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