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Home  > 2-(3-Bromoquinolin-6-yl)acetic acid

AA08768

1022091-93-5 | 2-(3-Bromoquinolin-6-yl)acetic acid

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $315.00 $220.00 -   +
250mg 95% in stock $589.00 $412.00 -   +
1g 95% in stock $1,462.00 $1,023.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AA08768
Chemical Name: 2-(3-Bromoquinolin-6-yl)acetic acid
CAS Number: 1022091-93-5
Molecular Formula: C11H8BrNO2
Molecular Weight: 266.0907
MDL Number: MFCD17215805
SMILES: OC(=O)Cc1ccc2c(c1)cc(cn2)Br

 

Computed Properties
Complexity: 247  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 2  
XLogP3: 2.3  

 

 

Upstream Synthesis Route
  • The 2-(3-Bromoquinolin-6-yl)acetic acid is a versatile compound widely used in chemical synthesis. Its unique structure makes it a valuable building block for the generation of diverse molecules with potential applications in pharmaceuticals, agrochemicals, and materials science.In chemical synthesis, 2-(3-Bromoquinolin-6-yl)acetic acid serves as a key intermediate for the preparation of various heterocyclic compounds. Its quinoline ring system offers opportunities for the introduction of functional groups through substitution reactions, enabling the creation of structurally complex molecules. Additionally, the presence of the carboxylic acid group provides a handle for further derivatization, allowing for the modulation of its chemical properties.Furthermore, 2-(3-Bromoquinolin-6-yl)acetic acid can participate in cross-coupling reactions, such as Suzuki-Miyaura or Heck coupling, to forge carbon-carbon bonds with other organic entities. This enables the formation of biaryl or alkylated products, expanding the chemical space accessible for exploration.Overall, the strategic incorporation of 2-(3-Bromoquinolin-6-yl)acetic acid in chemical synthesis facilitates the construction of structurally diverse and functionally rich molecules, offering a pathway towards the discovery of novel compounds with potential biological or materials-related activities.
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