The Chemistry of 2-Amino-3,4-difluorobenzonitrile: Synthesis and Applications
The realm of organic chemistry is rich with versatile molecules that serve as foundational blocks for creating advanced materials and life-saving pharmaceuticals. Among these, aromatic compounds featuring specific functional groups and halogenation patterns are of particular interest. 2-Amino-3,4-difluorobenzonitrile, identified by CAS number 1384265-40-0, is one such compound, offering a unique combination of an amino group, a nitrile, and two fluorine atoms on a benzene ring, making it a valuable intermediate in numerous chemical processes.
Chemical Structure and Properties
2-Amino-3,4-difluorobenzonitrile has the molecular formula C7H4F2N2 and a molecular weight of 154.12 g/mol. Its structure features a benzonitrile core substituted with an amine group at the ortho position and two fluorine atoms at the meta and para positions relative to the amine. This specific arrangement of functional groups dictates its reactivity and suitability for various synthetic transformations. Typically presented as an off-white solid, it is often stored under specific conditions, such as in a dark place under an inert atmosphere at 2-8°C, to maintain its purity and integrity.
Synthesis Pathways and Manufacturing
The synthesis of 2-Amino-3,4-difluorobenzonitrile typically involves multi-step organic reactions. While specific patented routes may vary, general approaches often begin with appropriately substituted difluorobenzene derivatives. These processes require precise control of reaction conditions, including temperature, pressure, and reagent stoichiometry, to achieve high yields and purity. For industrial-scale production, manufacturers focus on optimizing these parameters to ensure cost-effectiveness and consistent product quality, meeting demands for high purity intermediates often specified at 97% or higher.
Diverse Applications in Chemical Synthesis
The presence of both an electron-donating amino group and an electron-withdrawing nitrile group, coupled with the electronegativity of fluorine atoms, makes 2-Amino-3,4-difluorobenzonitrile a highly reactive and adaptable building block. Its applications are widespread:
- Pharmaceutical Intermediates: It is frequently used in the synthesis of pharmaceutical agents. The fluorine atoms can enhance metabolic stability, increase lipophilicity, and influence binding interactions with biological targets, leading to improved drug efficacy.
- Agrochemical Synthesis: Similar to pharmaceuticals, the incorporation of fluorinated motifs can enhance the effectiveness and environmental persistence of pesticides and herbicides.
- Materials Science: The unique electronic and structural properties imparted by the difluorobenzonitrile moiety make it relevant in the development of advanced materials, including components for organic electronics and specialty polymers.
- Research and Development: As a versatile intermediate, it is invaluable for academic and industrial researchers exploring novel synthetic routes and developing new chemical entities.
Procurement from a Reliable Manufacturer
For businesses requiring 2-Amino-3,4-difluorobenzonitrile, partnering with a reputable manufacturer and supplier is crucial. Factors such as consistent product quality, guaranteed purity levels, competitive pricing, and timely delivery are essential. We pride ourselves on being a trusted source for high-quality chemical intermediates. We encourage procurement professionals and R&D scientists to engage with us to request a quote and explore sample options, ensuring you have a reliable supply for your critical synthesis needs.
Perspectives & Insights
Agile Reader One
“2-Amino-3,4-difluorobenzonitrile, identified by CAS number 1384265-40-0, is one such compound, offering a unique combination of an amino group, a nitrile, and two fluorine atoms on a benzene ring, making it a valuable intermediate in numerous chemical processes.”
Logic Vision Labs
“Chemical Structure and Properties 2-Amino-3,4-difluorobenzonitrile has the molecular formula C7H4F2N2 and a molecular weight of 154.”
Molecule Origin 88
“Its structure features a benzonitrile core substituted with an amine group at the ortho position and two fluorine atoms at the meta and para positions relative to the amine.”