Aclonifen

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Identification

Molecular formula
C12H6Cl2N2
CAS Number
74070-46-5
IUPAC Name
3-(3,5-dichlorophenyl)-2-(3-pyridyl)prop-2-enenitrile
Molecular Weight
288.10g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3810g/cm3
Synonyms
Tyrphostin RG 14620
Interesting facts

Exploring 3-(3,5-Dichlorophenyl)-2-(3-pyridyl)prop-2-enenitrile

3-(3,5-Dichlorophenyl)-2-(3-pyridyl)prop-2-enenitrile is a complex organic compound that showcases fascinating structural features and potential applications in various fields.

Unique Structural Characteristics

  • Diverse Functionality: This compound incorporates a pyridine ring, which is known for its aromatic nature and ability to participate in a wide range of chemical reactions.
  • Chlorinated Aromatic System: The presence of 3,5-dichlorophenyl contributes both to the compound's stability and its reactivity, making it an interesting subject for synthetic organic chemistry.
  • Ability to Form Complexes: The pyridine moiety can coordinate with metals, making this compound a potential ligand in coordination chemistry.

Applications and Uses

This compound has garnered interest for several reasons:

  • Pharmaceutical Potential: The structural motifs present may lend themselves to the development of new pharmaceuticals, particularly as antitumor agents.
  • Material Science: The unique properties of this compound may find applications in the development of advanced materials, including organic light-emitting diodes (OLEDs).
  • Pest Control: Chlorinated compounds are often investigated for their insecticidal properties, suggesting potential utility in agrochemicals.

Chemical Behavior and Reactions

The electrophilic aromatic substitution reactions and nucleophilic addition mechanisms associated with this compound can lead to the synthesis of various derivatives, significantly expanding its chemical library. In addition, the nitrile group can undergo hydrolysis to yield carboxylic acids or be utilized in further reaction sequences to create amines or other functional groups, thereby making it a versatile building block in organic synthesis.

Conclusion

In summary, 3-(3,5-dichlorophenyl)-2-(3-pyridyl)prop-2-enenitrile represents a noteworthy example of how complex organic compounds can have rich chemical behavior and multiple avenues for research and applications. Whether as a novel pharmaceutical, a component in advanced materials, or a tool in agrochemistry, this compound holds potential that is just beginning to be explored.

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