1-Naphthol, or α-naphthol, is a organic compound with the formula C₁₀H₇OH. It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are precursors to a variety of useful compounds.^[2]

Quick Facts Names, Identifiers ...

1-Naphthol

Names
Preferred IUPAC name Naphthalen-1-ol
Other names 1-Hydroxynaphthalene; 1-Naphthalenol; α-Naphthol
Identifiers
CAS Number	90-15-3 Y
3D model (JSmol)	Interactive image
Beilstein Reference	1817321
ChEBI	CHEBI:10319 Y
ChEMBL	ChEMBL122617 Y
ChemSpider	6739 Y
ECHA InfoCard	100.001.791
EC Number	201-969-4
Gmelin Reference	69192
KEGG	C11714 Y
PubChem CID	7005
UNII	2A71EAQ389 Y
CompTox Dashboard (EPA)	DTXSID6021793
InChI InChI=1S/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H Y Key: KJCVRFUGPWSIIH-UHFFFAOYSA-N Y InChI=1/C10H8O/c11-10-7-3-5-8-4-1-2-6-9(8)10/h1-7,11H Key: KJCVRFUGPWSIIH-UHFFFAOYAZ
SMILES Oc2cccc1ccccc12
Properties
Chemical formula	C10H8O
Molar mass	144.17 g/mol
Appearance	Colorless or white solid
Density	1.10 g/cm3
Melting point	95 to 96 °C (203 to 205 °F; 368 to 369 K)
Boiling point	278 to 280 °C (532 to 536 °F; 551 to 553 K)
Magnetic susceptibility (χ)	-98.2·10−6 cm3/mol
Hazards
GHS labelling:[1]
Pictograms
Signal word	Danger
Hazard statements	H302, H311, H312, H315, H317, H318, H335, H410, H412
Precautionary statements	P261, P262, P264, P264+P265, P270, P271, P272, P273, P280, P301+P317, P302+P352, P304+P340, P305+P354+P338, P316, P317, P319, P321, P330, P332+P317, P333+P317, P361+P364, P362+P364, P391, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Y verify (what is YN ?) Infobox references

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1-Naphthol is prepared by two main routes.^[2] In one method, naphthalene is nitrated to give 1-nitronaphthalene, which is hydrogenated to the amine followed by hydrolysis:

C₁₀H₈ + HNO₃ → C₁₀H₇NO₂ + H₂O

C₁₀H₇NO₂ + 3H₂ → C₁₀H₇NH₂ + 2H₂O

C₁₀H₇NH₂ + H₂O → C₁₀H₇OH + NH₃

Alternatively, naphthalene is hydrogenated to tetralin, which is oxidized to 1-tetralone, which undergoes dehydrogenation.

Some reactions of 1-naphthol are explicable with reference to its tautomerism, which produces a small amount of the keto tautomer.

One consequence of this tautomerism is the Bucherer reaction, the ammonolysis of 1-naphthol to give 1-aminonaphthalene.

1-Naphthol biodegrades via formation of 1-naphthol-3,4-oxide, which converts to 1,4-naphthoquinone.^[3]

The 4-position of 1-naphthol is susceptible to electrophilic attack. This regioselective reaction is exploited in the preparation of diazo dyes, which are form using diazonium salts. Reduction of the diazo derivatives gives 4-amino-1-naphthol.^[4][5]

Partial reduction of 1-naphthol gives the tetrahydro derivative, leaving intact the phenol ring.^[6] Full hydrogenation is catalyzed by rhodium.^[7]

1-Naphthol is a precursor to a variety of insecticides including carbaryl and pharmaceuticals including nadolol^[8][9] as well as for the antidepressant sertraline^[10] and the anti-protozoan therapeutic atovaquone.^[11] It undergoes azo coupling to give various azo dyes, but these are generally less useful than those derived from 2-naphthol.^[2][12]

1-Naphthol is a metabolite of the insecticide carbaryl and naphthalene. Along with TCPy, it has been shown to decrease testosterone levels in adult men.^[13]

1-Naphthol has been described as "moderately toxic.^[2]