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AB70215

57798-00-2 | 8-Bromoquinolin-4(1H)-one

Packsize Purity Availability Price Discounted Price    Quantity
1g 95% in stock $30.00 $21.00 -   +
5g 95% in stock $42.00 $30.00 -   +
10g 95% in stock $73.00 $52.00 -   +
25g 95% in stock $163.00 $115.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB70215
Chemical Name: 8-Bromoquinolin-4(1H)-one
CAS Number: 57798-00-2
Molecular Formula: C9H6BrNO
Molecular Weight: 224.054
MDL Number: MFCD00272389
SMILES: Oc1ccnc2c1cccc2Br

 

Computed Properties
Complexity: 227  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 2.2  

 

 

Upstream Synthesis Route
  • 8-Bromoquinoline-4-ol, also known as 8-BQ4-OH, is a versatile chemical compound that finds widespread application in chemical synthesis. This compound serves as a valuable building block in the creation of various organic molecules due to its unique structural properties.One key application of 8-Bromoquinoline-4-ol in chemical synthesis is as a precursor in the preparation of heterocyclic compounds. By using 8-Bromoquinoline-4-ol as a starting material, chemists can introduce specific functional groups and manipulate the structure to synthesize complex molecules with desired properties. The presence of the quinoline ring in 8-Bromoquinoline-4-ol imparts distinct reactivity and allows for diverse functionalization strategies, making it a valuable intermediate in organic synthesis.Additionally, 8-Bromoquinoline-4-ol can be utilized as a key reagent in the synthesis of pharmaceuticals and agrochemicals. Its ability to undergo various chemical transformations, such as halogenation, alkylation, and Suzuki coupling, makes it a valuable tool for the preparation of bioactive compounds with potential therapeutic or agricultural applications. The presence of the hydroxyl group in 8-Bromoquinoline-4-ol further expands its utility by enabling additional derivatization and modification for specific target molecules.Overall, 8-Bromoquinoline-4-ol stands as a crucial component in the toolbox of synthetic chemists, offering a wide range of possibilities for the construction of diverse organic compounds with tailored functionalities and applications.
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