AA80648
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
250mg | 97% | in stock | $106.00 | $75.00 | - + | |
1g | 97% | in stock | $267.00 | $187.00 | - + | |
5g | 97% | in stock | $760.00 | $532.00 | - + | |
10g | 97% | in stock | $1,319.00 | $923.00 | - + | |
25g | 97% | in stock | $2,625.00 | $1,837.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AA80648 |
Chemical Name: | 6-(Bromomethyl)nicotinonitrile |
CAS Number: | 158626-15-4 |
Molecular Formula: | C7H5BrN2 |
Molecular Weight: | 197.032 |
MDL Number: | MFCD11227190 |
SMILES: | BrCc1ccc(cn1)C#N |
Complexity: | 149 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 1 |
XLogP3: | 1.2 |
6-(Bromomethyl)nicotinonitrile is a versatile compound that finds widespread application in organic synthesis. Its unique structure containing a bromomethyl group attached to the nicotinonitrile moiety lends itself well to various chemical transformations, making it a valuable building block for the preparation of diverse organic molecules.One key aspect of its utility lies in its role as a reactive intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The bromomethyl group can serve as a handle for further functionalization through substitution, coupling, or elimination reactions. This allows for the introduction of additional functional groups or structural modifications to tailor the properties of the final molecule for specific applications.Moreover, 6-(Bromomethyl)nicotinonitrile can participate in cross-coupling reactions with various nucleophiles or undergo cyclization processes to form heterocyclic compounds. These transformations enable the creation of complex molecular scaffolds with precise control over regioselectivity and stereochemistry, facilitating the development of new drug candidates or advanced materials.Overall, the strategic incorporation of 6-(Bromomethyl)nicotinonitrile into synthetic routes offers chemists a powerful tool to access a diverse array of structurally diverse compounds with potential therapeutic, agricultural, or industrial relevance. By harnessing its reactivity and versatility, researchers can expedite the discovery and optimization of bioactive molecules or functional materials with enhanced properties and performance.