4-Nitrophenol (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "4-Nitrophenol" in English language version.

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cdc.gov

Toxicological Profile For Nitrophenols (PDF) (Report). Agency for Toxic Substances and Disease Registry, U.S. Public Health Service. July 1992.

This is no longer a recommended IUPAC name: Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 690. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4. Only one name is retained, phenol, for C₆H₅-OH, both as a preferred name and for general nomenclature. The structure is substitutable at any position. Locants 2, 3, and 4 are recommended, not o, m, and p.
Bowers, G.N.; McComb, R.B.; Christensen, R.C.; Schaffer, R. (1980). "High-Purity 4-Nitrophenol: Purification, Characterization, and Specifications for Use as a Spectrophotometric Reference Material". Clinical Chemistry. 26 (6): 724–729. doi:10.1093/clinchem/26.6.724. PMID 7371150.
Biggs, A.I. (1954). "A spectrophotometric determination of the dissociation constants of p-nitrophenol and papaverine". Transactions of the Faraday Society. 50 (50): 800–802. doi:10.1039/tf9545000800.

"4-Nitrophenol CAS 100-02-7 | 106798". www.merckmillipore.com. Retrieved 2016-10-28.