4-나이트로페놀 (Korean Wikipedia)

Analysis of information sources in references of the Wikipedia article "4-나이트로페놀" in Korean language version.

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3doi.org

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2archive.org

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2nih.gov

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1merckmillipore.com

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1clinchem.org

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1shimadzu.com

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1cdc.gov

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archive.org (Global: 6^th place; Korean: 18^th place)

Ellis, Frank (2002). 《Paracetamol: a curriculum resource》. Cambridge: Royal Society of Chemistry. ISBN 0-85404-375-6.
Ninfa, Alexander (2010). 《Fundamental Laboratory Approached for Biochemistry and Biotechnology》. Wiley. 153, 243쪽. ISBN 978-0470087664.

cdc.gov (Global: 218^th place; Korean: 52^nd place)

atsdr.cdc.gov

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

clinchem.org (Global: low place; Korean: 5,690^th place)

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.

doi.org (Global: 2^nd place; Korean: 3^rd place)

dx.doi.org

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. 690쪽. 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.

merckmillipore.com (Global: 9,664^th place; Korean: low place)

“4-Nitrophenol CAS 100-02-7 | 106798”. 《www.merckmillipore.com》. 2016년 10월 28일에 확인함.

nih.gov (Global: 4^th place; Korean: 4^th place)

toxnet.nlm.nih.gov

“TOXNET”. 《toxnet.nlm.nih.gov》. 2016년 10월 28일에 확인함.

ncbi.nlm.nih.gov

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.

shimadzu.com (Global: low place; Korean: low place)

“The Relationship Between UV-VIS Absorption and Structure of Organic Compounds”. 《Shimadzu》. 2017년 5월 14일에 확인함.

4-나이트로페놀 (Korean Wikipedia)

archive.org (Global: 6th place; Korean: 18th place)

cdc.gov (Global: 218th place; Korean: 52nd place)

atsdr.cdc.gov

clinchem.org (Global: low place; Korean: 5,690th place)

doi.org (Global: 2nd place; Korean: 3rd place)

dx.doi.org

merckmillipore.com (Global: 9,664th place; Korean: low place)

nih.gov (Global: 4th place; Korean: 4th place)

toxnet.nlm.nih.gov

ncbi.nlm.nih.gov

shimadzu.com (Global: low place; Korean: low place)

archive.org (Global: 6^th place; Korean: 18^th place)

cdc.gov (Global: 218^th place; Korean: 52^nd place)

clinchem.org (Global: low place; Korean: 5,690^th place)

doi.org (Global: 2^nd place; Korean: 3^rd place)

merckmillipore.com (Global: 9,664^th place; Korean: low place)

nih.gov (Global: 4^th place; Korean: 4^th place)