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9,10-Phenanthrenequinon may be used for high quality passivation on silicon (100) surfaces. Quinones may serve as substrates for a variety of flavoenzymes, useful fluorescent compound and quinone. Also used in dyes, as a hardener for dental restoration, for the determination of copper by spectrophotometric method, and for organic synthesis.
Avasthi, Sushobhan, et al. Electronic structure and band alignment of 9, 10-phenanthrenequinone passivated silicon surfaces. Surface Science., 2011, 605 (13), 1308-1312.
P L Chesis; D E Levin; M T Smith; L Ernster; B N Ames. Mutagenicity of quinones: pathways of metabolic activation and detoxification. PNAS, 1984, 81 (6), 1696-1700.
Specific, highly sensitive reagent for arginine and arginyl peptides: Biochem. Biophys. Acta, 130, 538 (1966).
Reagent for dehydrogenation, e.g. of thiazolines to thiazoles in high yield: J. Chem. Soc.(C), 1061 (1966). Review: Chem. Rev., 78, 317 (1978).
Like 1,2-Cyclohexanedione, A14401, has been used by Ley's group for protection of trans-1,2-diols as cyclic diacetals. The method is particularly applicable to the carbohydrate field: Synlett, 793 (1996); J. Chem. Soc., Perkin 1, 2023 (1997):
Gefahrenhinweise (EU): H319
Causes serious eye irritation.
Wear eye/face protection. Wash thoroughly after handling. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If eye irritation persists: Get medical advice/attention.