• 1. An asymmetric supercapacitor based on controllable WO3 nanorod bundle and alfalfa-derived porous carbon?
  Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
• 2. An anti-ultrasonic-stripping effect in confined micro/nanoscale cavities and its applications for efficient multiscale metallic patterning?
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• 3. An amplified fluorescence detection of T4 polynucleotide kinase activity based on coupled exonuclease III reaction and a graphene oxide platform?
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• 4. An atmosphere and light tuned highly diastereoselective synthesis of cyclobuta/penta[b]indoles from aniline-tethered alkylidenecyclopropanes with alkynes?
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• 5. An interplay between electronic and structural effects on the photoluminescence decay mechanisms in LaPO4·nH2O:Tb3+ and LaPO4:Tb3+ single-crystal nanorods?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Biphenyls and derivatives Biphenylcarbonitriles

Comprehensive Overview of [1,1'-Biphenyl]-4-carbonitrile,4'-(nonyloxy)- (CAS No. 58932-13-1)

[1,1'-Biphenyl]-4-carbonitrile,4'-(nonyloxy)- is a specialized organic compound with the CAS number 58932-13-1, widely recognized for its unique chemical structure and applications in advanced material science. This compound belongs to the biphenyl family, featuring a cyano group at the 4-position and a nonyloxy substituent at the 4'-position. Its molecular formula is C₂₂H₂₇NO, and it exhibits properties that make it valuable in liquid crystal displays (LCDs), organic semiconductors, and photovoltaic materials.

In recent years, the demand for high-performance organic materials has surged, driven by advancements in flexible electronics and renewable energy technologies. Researchers and manufacturers are increasingly focusing on compounds like [1,1'-Biphenyl]-4-carbonitrile,4'-(nonyloxy)- due to its thermal stability and electrochemical properties. These characteristics are critical for developing next-generation OLEDs (Organic Light-Emitting Diodes) and solar cells, aligning with global trends toward sustainability and energy efficiency.

The synthesis of [1,1'-Biphenyl]-4-carbonitrile,4'-(nonyloxy)- involves multi-step organic reactions, including cross-coupling and etherification processes. Its nonyloxy chain enhances solubility in organic solvents, facilitating its integration into thin-film coatings and polymer matrices. This adaptability has sparked interest in its potential for printed electronics, a rapidly growing sector aiming to reduce production costs and environmental impact.

From an industrial perspective, 58932-13-1 is often discussed in the context of material innovation and green chemistry. Companies are exploring its use in biodegradable electronics, addressing concerns about e-waste and resource depletion. Additionally, its role in optoelectronic devices has been highlighted in academic studies, particularly for improving charge transport efficiency and device longevity.

For researchers and professionals seeking detailed information, [1,1'-Biphenyl]-4-carbonitrile,4'-(nonyloxy)- is frequently referenced in patents and journals related to advanced functional materials. Its CAS registry number (58932-13-1) serves as a key identifier in databases like SciFinder and Reaxys, ensuring accurate retrieval of technical data. As the push for eco-friendly technologies intensifies, this compound is poised to play a pivotal role in shaping the future of smart materials and sustainable electronics.

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