AD50113
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 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
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 |
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 |
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.