• 1. An air-stable organometallic polymer containing titanafluorene moieties obtained by the Sonogashira–Hagihara cross-coupling polycondensation?
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• 2. An analyte-triggered artificial peroxidase system based on dimanganese complex for a versatile enzyme assay?
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• 3. An alkynylboronatecycloaddition strategy to functionalised benzyne derivatives?
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• 4. An approach towards the synthesis of novel fused nitrogen tricyclic heterocyclic scaffolds via GBB reaction?
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• 5. An antimonate pyrochlore (H1.23Sr0.45SbO3.48) for photocatalytic oxidation of benzene: effective oxygen usage and excellent activity?
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Comprehensive Overview of N-(2-Cyanoethyl)-N-ethyl-m-toluidine (CAS No. 148-69-6): Properties, Applications, and Industry Insights

N-(2-Cyanoethyl)-N-ethyl-m-toluidine (CAS No. 148-69-6) is a specialized organic compound widely recognized for its role in fine chemical synthesis and industrial applications. This aromatic amine derivative features a cyanoethyl group and an ethyl substituent attached to a meta-toluidine backbone, making it a versatile intermediate in the production of dyes, pharmaceuticals, and advanced materials. Its molecular structure (C₁₂H₁₆N₂) and functional groups contribute to unique reactivity, enabling applications in cross-coupling reactions and polymer stabilization.

In recent years, the demand for N-(2-Cyanoethyl)-N-ethyl-m-toluidine has surged due to its utility in high-performance polymers and electronic materials. Researchers and manufacturers frequently search for "CAS 148-69-6 solubility" or "synthesis of N-ethyl-m-toluidine derivatives," reflecting its relevance in R&D. The compound’s compatibility with photoresist formulations has also sparked interest in semiconductor fabrication, aligning with trends in miniaturized electronics and green chemistry.

From a technical perspective, 148-69-6 exhibits moderate polarity, with a melting point range of 60–65°C and stability under inert atmospheres. Its cyano group enhances electrophilic properties, facilitating nucleophilic substitutions—a feature exploited in agrochemical intermediates. Environmental considerations have led to studies on its biodegradability, addressing queries like "eco-friendly alternatives to toluidine derivatives." Regulatory compliance (e.g., REACH) further underscores its safe handling protocols.

Innovative applications include its use as a UV absorber in coatings and as a ligand precursor in catalytic systems. The compound’s synergy with nanoparticle synthesis has been explored in peer-reviewed journals, responding to searches such as "CAS 148-69-6 in nanotechnology." As industries prioritize sustainable sourcing, suppliers now highlight high-purity grades (>98%) with reduced heavy-metal content.

In summary, N-(2-Cyanoethyl)-N-ethyl-m-toluidine bridges traditional chemistry and cutting-edge technology. Its adaptability to green synthesis methods and alignment with circular economy principles position it as a compound of enduring significance. For researchers, understanding its structure-activity relationship remains key to unlocking novel applications in material science and beyond.

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• 119-95-9(3-(2-Hydroxyethyl)(3-methylphenyl)aminopropanenitrile)
• 148-87-8(3-(Ethylphenylamino)propanenitrile)
• 1555-66-4(N,N-Bis(2-cyanoethyl)aniline)
• 36034-62-5(3-(3,5-dimethylphenyl)aminopropanenitrile)
• 17601-74-0(3-(Phenethyl(phenyl)amino)propanenitrile)
• 27618-25-3(3-(m-Toluidino)propiononitrile)
• 18934-20-8(3,3'-((3-methylphenyl)imino)bispropanenitrile)
• 1077-24-3(3-(4-Methylphenyl)aminopropanenitrile)
• 63817-48-1(Propanenitrile, 3-[(3-methylphenyl)(2-phenylethyl)amino]-)