Why 2-(Trifluoromethyl)-5-Nitrobenzonitrile is a Top Choice for Chemical Suppliers
In the vast catalog of chemical intermediates, certain compounds rise to prominence due to their versatility, unique structural features, and broad applicability. 2-(Trifluoromethyl)-5-Nitrobenzonitrile (CAS: 887350-95-0) is one such molecule that commands attention from chemical suppliers and researchers alike. Its combination of a trifluoromethyl group, a nitro group, and a nitrile functionality on an aromatic ring makes it a valuable commodity for numerous synthetic endeavors.
A Trifecta of Reactivity: CF₃, NO₂, CN
The appeal of 2-(Trifluoromethyl)-5-Nitrobenzonitrile as a chemical intermediate stems directly from the reactivity and utility of its constituent functional groups:
- Trifluoromethyl (CF₃) Group: This highly electronegative and lipophilic group is a staple in modern drug discovery and agrochemical design. Its inclusion can enhance metabolic stability, improve bioavailability, and modulate receptor binding affinity. Compounds featuring this moiety are consistently in demand.
- Nitro (NO₂) Group: A powerful electron-withdrawing group, the nitro moiety activates aromatic rings for nucleophilic substitution and, crucially, can be readily reduced to an amine. This amine then serves as a critical handle for building more complex molecular architectures through a wide array of synthetic transformations.
- Nitrile (CN) Group: The nitrile functionality offers another versatile point of modification. It can be hydrolyzed to carboxylic acids or amides, or reduced to primary amines, further expanding the synthetic possibilities and the range of accessible downstream products.
This synergistic combination of functional groups makes 2-(Trifluoromethyl)-5-Nitrobenzonitrile a highly sought-after building block for synthesizing complex organic molecules used in pharmaceuticals, agrochemicals, and advanced materials.
Meeting the Demand: Purity, Price, and Availability
For chemical suppliers, offering a compound like 2-(Trifluoromethyl)-5-Nitrobenzonitrile requires a robust understanding of market needs. Researchers and industrial clients seek not only the compound itself but also assurance of its quality, competitive pricing, and reliable availability. A high assay (like the ≥98.0% purity standard) is non-negotiable for critical synthetic steps. Furthermore, the ability to provide this intermediate at a competitive price, particularly for bulk quantities, is essential for its adoption in large-scale manufacturing. As a dedicated manufacturer, we prioritize these aspects, ensuring that when you choose to buy 2-(Trifluoromethyl)-5-Nitrobenzonitrile from us, you are partnering with a supplier committed to supporting your research and production goals.
Applications Driving Demand
The demand for 2-(Trifluoromethyl)-5-Nitrobenzonitrile is driven by its application in several high-value sectors:
- Pharmaceutical Synthesis: It serves as a key intermediate for novel APIs where fluorinated aromatic rings are desired.
- Agrochemical Development: Its structural features make it suitable for creating advanced pesticides and herbicides.
- Fine Chemical Production: It enables the synthesis of specialized chemicals with tailored properties.
The consistent demand from these industries underscores why 2-(Trifluoromethyl)-5-Nitrobenzonitrile remains a top choice for chemical suppliers looking to offer essential building blocks for modern chemical synthesis. If you are looking for a reliable source to buy this compound or to request a quote, explore the advantages of working with an experienced manufacturer.
Perspectives & Insights
Bio Analyst 88
“2-(Trifluoromethyl)-5-Nitrobenzonitrile (CAS: 887350-95-0) is one such molecule that commands attention from chemical suppliers and researchers alike.”
Nano Seeker Pro
“Its combination of a trifluoromethyl group, a nitro group, and a nitrile functionality on an aromatic ring makes it a valuable commodity for numerous synthetic endeavors.”
Data Reader 7
“Its inclusion can enhance metabolic stability, improve bioavailability, and modulate receptor binding affinity.”