1,5-Dihydroxynaphthalene

1,5-Dihydroxynaphthalene
Names
	IUPAC name Naphthalene-1,5-diol
	Other names Azurol; 1,5-Naphthalenediol
Identifiers
CAS Number	83-56-7 ;
3D model (JSmol)	Interactive image;
ChemSpider	6492;
ECHA InfoCard	100.001.353
PubChem CID	6749;
UNII	P25HC23VH6 ;
CompTox Dashboard (EPA)	DTXSID2052574 ;
	InChI InChI=1S/C10H8O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1-6,11-12H Key: BOKGTLAJQHTOKE-UHFFFAOYSA-N; InChI=1/C10H8O2/c11-9-5-1-3-7-8(9)4-2-6-10(7)12/h1-6,11-12H Key: BOKGTLAJQHTOKE-UHFFFAOYAJ;
	SMILES c1cc2c(cccc2O)c(c1)O;
Properties
Chemical formula	C10H8O2
Molar mass	160.172 g·mol−1
Appearance	Colorless solid
Melting point	259–261 °C (498–502 °F; 532–534 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

1,5-Dihydroxynaphthalene is an organic compound with the formula C₁₀H₆(OH)₂. It is one of several isomers of dihydroxynaphthalene. It exists as colorless crystals that are soluble in polar organic solvents. It is a precursor to certain dyes.

Preparation and use

1,5-Dihydroxynaphthalene is prepared from naphthalene-1,5-disulfonic acid by hydrolysis with strong base followed by acidification.

It couples with various aryl diazonium salts to give diazo dyes. Oxidation with chromium trioxide gives juglone, a naturally occurring dye.[1]

gollark: ++apioform

References

Gerald Booth (2005). "Naphthalene Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_009..

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[Ullmann-1] Gerald Booth (2005). "Naphthalene Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a17_009..