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AD50113

103030-25-7 | 6-(Bromomethyl)quinoline hydrobromide

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% in stock $58.00 $40.00 -   +
250mg 97% in stock $86.00 $60.00 -   +
1g 97% in stock $116.00 $81.00 -   +
5g 97% in stock $477.00 $334.00 -   +
10g 97% in stock $881.00 $617.00 -   +
25g 97% in stock $2,184.00 $1,529.00 -   +

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*All prices are in USD.

Description
Catalog Number: AD50113
Chemical Name: 6-(Bromomethyl)quinoline hydrobromide
CAS Number: 103030-25-7
Molecular Formula: C10H9Br2N
Molecular Weight: 302.99316
MDL Number: MFCD22200057
SMILES: BrCc1ccc2c(c1)cccn2.Br

 

Computed Properties
Complexity: 149  
Covalently-Bonded Unit Count: 2  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 1  
Rotatable Bond Count: 1  

 

 

Upstream Synthesis Route
  • 6-(Bromomethyl)quinoline hydrobromide is a versatile compound widely used in chemical synthesis as a key reagent in numerous reactions. With its unique structure, this compound serves as a crucial building block in the production of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 6-(Bromomethyl)quinoline hydrobromide plays a vital role in the functionalization of quinoline derivatives, enabling the introduction of bromomethyl groups into complex molecules. This reagent is particularly useful in the synthesis of heterocyclic compounds and versatile intermediates, allowing chemists to access diverse chemical space and create novel structures with desirable properties.Furthermore, the presence of the bromomethyl group in 6-(Bromomethyl)quinoline hydrobromide enhances the reactivity of the quinoline core, facilitating substitution reactions, cross-coupling reactions, and other transformations. This compound's ability to undergo selective reactions makes it a valuable tool for chemists seeking to modify quinoline-based molecules with precision and efficiency.Overall, the application of 6-(Bromomethyl)quinoline hydrobromide in chemical synthesis showcases its importance as a strategic reagent for expanding the synthetic toolbox and enabling the creation of diverse organic compounds with potential applications in pharmaceuticals, materials science, and beyond.
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