≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
🌡
Storage & shipping
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
📋
Quality documents
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
📚
Literature proof
Cited in 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Descripción general
4-Cyanophenylboronic acid can be used as a reactant in: Palladium-catalyzed Suzuki-Miyaura cross-coupling in water. Ruthenium catalyzed direct arylation of benzylic sp3 carbons of acyclic amines with arylboronates. Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids. Ferric perchlorate-promoted reaction of fullerenes with various arylboronic acids to give fullerenyl boronic esters. Phosphine-free Suzuki-Miyaura cross-coupling. Palladacycles as effective catalysts for multicomponent reaction with allylpalladium-intermediates. Chan-Lam-type Cu-catalyzed S-arylation of thiols. Regioselective cross-coupling reactions under modfied Suzuki and Still cross-coupling reactions with copper catalysis. Metal-free biaryl coupling reaction in the presence of dimethyl carbonate as a solvent. Suzuki-type cross-coupling reaction with pentavalent triarylantimony diacetates in the absence of a base. It can also be used to prepare: Himbacine analogs as thrombin receptor antagonists and potential antiplatelet agents. Trisulfonated calixarene upper-rim sulfonamido and their complexation with trimethyllysine epigenetic mark. Antimalarial compounds via Suzuki cross-coupling. Deoxyuridine derivatives. Reactant involved in: Oxidative hydroxylation Trifluoromethylation 1,4-Addition reactions Precursor in the synthesis of inhibitors such as: Tpl2 kinase inhibitors P2X7 antagonists used in the treatment of pain
This compound belongs to the class of organic compounds known as benzonitriles. These are organic compounds containing a benzene bearing a nitrile substituent.
External Descriptors
Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
1.Shufang Liu, Ziqian Liu, Qing Su, Qiaolin Wu. (2022) Multifunctional covalent organic frameworks for photocatalytic oxidative hydroxylation of arylboronic acids and fluorescence sensing for Cu2+. MICROPOROUS AND MESOPOROUS MATERIALS, [PMID:][10.1016/j.micromeso.2022.111737]
2.Jianwen Tian, Muzhou Teng, Mu Song, Zhijia Li, Xiaoyong Zhang, Youqin Xu. (2021) A feasible molecular engineering for bright Π-conjugation free radical photosensitizers with aggregation-induced emission. DYES AND PIGMENTS, [PMID:][10.1016/j.dyepig.2021.109651]
3.Tao Ma, Feng Liang. (2020) Au–Pd Nanostars with Low Pd Content: Controllable Preparation and Remarkable Performance in Catalysis. Journal of Physical Chemistry C, [PMID:][10.1021/acs.jpcc.0c00031]
Calculadoras de soluciones
Molarity Calculator
Determine the necessary mass, volume, or concentration for preparing a solution.
Dilution Calculator
Determine the dilution needed to prepare a stock solution.
We use cookies to ensure the website functions properly and, where permitted, to improve your experience. You can manage your preferences at any time in Settings. Learn more in our Cookie Policy.
Shall we send you a message when we have discounts available?
Remind me later
Thank you! Please check your email inbox to confirm.
Products are supplied to verified businesses, institutions, and qualified professionals for research and development use only. Not for use in humans, animals, diagnosis, or therapy.
I2524246