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AA53918

1217500-61-2 | Oxindole-6-boronic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $43.00 $30.00 -   +
250mg 97% in stock $59.00 $41.00 -   +
1g 97% in stock $219.00 $154.00 -   +
5g 97% in stock $720.00 $504.00 -   +
25g 97% in stock $2,811.00 $1,968.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA53918
Chemical Name: Oxindole-6-boronic acid
CAS Number: 1217500-61-2
Molecular Formula: C8H8BNO3
Molecular Weight: 176.965
MDL Number: MFCD12913936
SMILES: O=C1Cc2c(N1)cc(cc2)B(O)O

 

Computed Properties
Complexity: 221  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 3  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • (2-Oxoindolin-6-yl)boronic acid is a versatile chemical compound widely used in organic synthesis due to its valuable reactivity and functional group tolerance. This compound serves as a key building block in the construction of various organic molecules, especially in the field of medicinal chemistry and materials science.In chemical synthesis, (2-Oxoindolin-6-yl)boronic acid can act as a valuable boron source, participating in various transformations such as Suzuki-Miyaura cross-coupling reactions. This enables the formation of carbon-carbon bonds in a controlled and efficient manner, essential for the assembly of complex molecular structures. The unique boronic acid functionality of this compound also allows for further derivatization, enabling the introduction of additional functional groups or modifications to tailor the properties of the resulting compounds.Additionally, (2-Oxoindolin-6-yl)boronic acid can serve as a useful intermediate in the synthesis of bioactive compounds, pharmaceuticals, agrochemicals, and advanced materials. Its structural versatility and compatibility with a wide range of reaction conditions make it a valuable tool for organic chemists seeking to access diverse chemical space and develop novel molecules with desired properties.Overall, the application of (2-Oxoindolin-6-yl)boronic acid in chemical synthesis offers a powerful and efficient approach to construct complex molecules, making it a valuable tool for researchers and synthetic chemists in various scientific fields.
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