AB44223
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
1g | 98% | in stock | $14.00 | $10.00 | - + | |
5g | 98% | in stock | $20.00 | $14.00 | - + | |
25g | 98% | in stock | $63.00 | $44.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AB44223 |
Chemical Name: | 2-Pyridylacetonitrile |
CAS Number: | 2739-97-1 |
Molecular Formula: | C7H6N2 |
Molecular Weight: | 118.1359 |
MDL Number: | MFCD00006346 |
SMILES: | N#CCc1ccccn1 |
Complexity: | 122 |
Covalently-Bonded Unit Count: | 1 |
Heavy Atom Count: | 9 |
Hydrogen Bond Acceptor Count: | 2 |
Rotatable Bond Count: | 1 |
XLogP3: | 0.6 |
2-Pyridylacetonitrile, also known as 2-cyanomethylpyridine, is a versatile chemical compound widely used in chemical synthesis. Its primary application lies in its role as a valuable building block in the preparation of various pharmaceuticals, agrochemicals, and fine chemicals.In chemical synthesis, 2-Pyridylacetonitrile serves as a key intermediate in the synthesis of heterocyclic compounds, particularly pyridine derivatives. Its unique structure containing both a pyridine ring and a nitrile group allows for diverse functional group transformations, making it a valuable starting material in organic synthesis.One of the notable applications of 2-Pyridylacetonitrile is its involvement in the synthesis of pyridine-based drugs and bioactive compounds. By functionalizing the nitrile group or modifying the pyridine ring, chemists can access a wide range of pharmacologically active molecules with potential therapeutic properties.Furthermore, 2-Pyridylacetonitrile can be utilized in metal-catalyzed cross-coupling reactions to construct complex molecular structures efficiently. Its electron-rich pyridine ring enables it to participate in various catalytic transformations, facilitating the formation of carbon-carbon and carbon-heteroatom bonds.Overall, 2-Pyridylacetonitrile's versatility and reactivity make it a valuable tool in the arsenal of synthetic chemists for the construction of diverse molecular architectures with applications across the pharmaceutical, agrochemical, and materials science industries.
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Molecules (Basel, Switzerland) 20091103
Acta crystallographica. Section E, Structure reports online 20090401
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Acta crystallographica. Section E, Structure reports online 20080801