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AA80648

158626-15-4 | 6-(Bromomethyl)nicotinonitrile

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 -   +

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*All prices are in USD.

Description
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

 

Computed Properties
Complexity: 149  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 10  
Hydrogen Bond Acceptor Count: 2  
Rotatable Bond Count: 1  
XLogP3: 1.2  

 

 

Upstream Synthesis Route
  • 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.
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