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Collect. Czech. Chem. Commun. 1971, 36, 3399-3403
https://doi.org/10.1135/cccc19713399

Reactivity of organic azo-compounds. XIII. Apparent dissociation constants of 4-phenylazo-1-naphthol derivatives in 50% (by vol.) ethanol

J. Schreiber, J. Kulič, J. Panchartek and M. Večeřa

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  • Wojciechowski Krzysztof, Szadowski Jerzy: Effect of the sulphonic group position on the properties of monoazo dyes. Dyes and Pigments 2000, 44, 137. <https://doi.org/10.1016/S0143-7208(99)00085-6>
  • Stoyanov Stefan, Antonov Liudmil, Soloveytchik Boriana, Petrova Veselina: Quantitative analysis of tautomeric equilibrium in 1-phenylazo-4-naphthols—a new approach. Dyes and Pigments 1994, 26, 149. <https://doi.org/10.1016/0143-7208(94)85008-9>
  • Ball P., Nicholls C.H.: Azo-hydrazone tautomerism of hydroxyazo compounds—a review. Dyes and Pigments 1982, 3, 5. <https://doi.org/10.1016/0143-7208(82)80010-7>
  • SCHREIBER J., KULIC J., PANCHARTEK J., VECERA M.: ChemInform Abstract: REAKTIVITAET VON ORGANISCHEN AZOVERBINDUNGEN 13. MITT. SCHEINBARE DISSOZIATIONSKONSTANTEN VON 4‐(X‐PHENYL‐AZO)‐1‐NAPHTHOL‐DEIVATEN IN 50 VOL.‐PROZENTIGEM AETHANOL. Chemischer Informationsdienst 1972, 3. <https://doi.org/10.1002/chin.197201092>