Chemistry:Naphthoquinone
From HandWiki
Naphthoquinones constitute a class of organic compounds (quinones) structurally related to naphthalene. The 1,2- and 1,4-isomers are common but others exist:[1]
- 1,2-Naphthoquinone
- 1,4-Naphthoquinone[2]
- 2,6-Naphthoquinone ({{{2}}})
Use and occurrence
Many natural products feature naphthoquinones, especially the 1,4 isomer.[3]
Amine-substituted naphthoquiones, e.g. Artisil Blue GFL and Helindon Yellow R, were once used as dyes.[4] Some interest remains in this area.[5]
See also
References
- ↑ Grolig, J.; Wagner, R.. "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_067.
- ↑ Caldwell, Erica; Deloux, Laurent; Srebnik, Morris (2001-04-15), John Wiley & Sons, Ltd, ed. (in en), 1,4-Naphthoquinone, Chichester, UK: John Wiley & Sons, Ltd, doi:10.1002/047084289x.rn001, ISBN 978-0-471-93623-7, https://onlinelibrary.wiley.com/doi/10.1002/047084289X.rn001, retrieved 2025-10-30
- ↑ Ahmadi, Esmaeil Sheikh; Tajbakhsh, Amir; Iranshahy, Milad; Asili, Javad; Kretschmer, Nadine; Shakeri, Abolfazl; Sahebkar, Amirhossein (2020-12-28). "Naphthoquinone Derivatives Isolated from Plants: Recent Advances in Biological Activity" (in en). Mini-Reviews in Medicinal Chemistry 20 (19): 2019–2035. doi:10.2174/1389557520666200818212020. PMID 32811411. https://www.eurekaselect.com/185045/article.
- ↑ Griffiths, John (2006). "Benzoquinone and Naphthoquinone Dyes". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_575.pub2. ISBN 978-3-527-30385-4.
- ↑ Dulo, Benson; Phan, Kim; Githaiga, John; Raes, Katleen; De Meester, Steven (December 2021). "Natural Quinone Dyes: A Review on Structure, Extraction Techniques, Analysis and Application Potential" (in en). Waste and Biomass Valorization 12 (12): 6339–6374. doi:10.1007/s12649-021-01443-9. ISSN 1877-2641. Bibcode: 2021WBioV..12.6339D. https://link.springer.com/10.1007/s12649-021-01443-9.
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