TCI C1299 4-Cyanobiphenyl combines a rigid, linear biphenyl core with a strongly polar nitrile group at the para position. This structural pairing makes it a classic reference scaffold in liquid crystal and optoelectronic materials research. The nitrile also serves as a synthetic handle for conversion into carboxylic acids, amides, primary amines, or tetrazoles. AMI Scientific supplies this TCI building block in 5 g and 25 g pack sizes for both characterisation and preparative work.
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- Takaguchi et al. (2009). Synthesis and Liquid Crystallinity of Fullerodendron Having Cyanobiphenyl Groups at the Terminals. ECS Meeting Abstracts doi:10.1149/ma2009-02/38/2849
- Yoshizawa et al. (2009). Biological Activity of Some Cyanobiphenyl Derivatives. Chemistry Letters doi:10.1246/cl.2009.530
- Sakuma (2012). Potential energy surface of 4-hexyl-4′-cyanobiphenyl (6CB) on graphite surface: a DFT study with van der Waals corrections. Molecular Simulation doi:10.1080/08927022.2011.557833
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
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