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2,3-Dihydroxynaphthalene

ALDRICH/37760 - ≥98.0% (HPLC)

Synonym: 2,3-Naphthalenediol

CAS Number: 92-44-4
Empirical Formula (Hill Notation): C10H8O2
Molecular Weight: 160.17
EC Number: 202-156-7
MDL Number: MFCD00004073
Linear Formula: C10H6(OH)2
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-37760-50G-F 50 g
$152.00
1/EA
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45-37760-250G-F 250 g
$235.00
1/EA
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assay ≥98.0% (HPLC)
InChI 1S/C10H8O2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,11-12H
InChI key JRNGUTKWMSBIBF-UHFFFAOYSA-N
mp 161-165 °C (lit.)
  162-164 °C
Quality Level 200 
SMILES string Oc1cc2ccccc2cc1O
sublimation residue ≤1%
Application: 2,3-Dihydroxynaphthalene may be used in the following studies:
• Construction of dinaphtho[2,1-b;2′,3′-d]furan-6-ol, via dehydration reaction in the presence of strong acid.
• As fused ring catecholate type ligand for the surface modification of nanocrystalline TiO2 particles.
• As adsorptive and competing ligand during the chemical speciation of iron in seawater by cathodic stripping voltammetry.
• Synthesis of cyclotriphosphazene derivatives, used as non-halogen flame retardants
General description: 2,3-Dihydroxynaphthalene is a polyhydroxy phenol. It is an aromatic dihydroxy compound having hydroxyl groups at ortho positions. Its reaction with molybdenum(VI) complexes has been reported. The asymmetric oxidative coupling polymerization of 2,3-dihydroxynaphthalene using the Cu(I)-bisoxazoline complex as catalyst has been reported to afford poly(2,3-dihydroxy-1,4-naphthylene), having a continuous 1,1′-bi-2-naphthol main chain structure. The nitrodisplacement reaction between nitrophthalodinitriles and 2,3-dihydroxynaphthalene has been investigated.
Packaging: 50, 250 g in poly bottle
Purity ≥98.0% (HPLC)
mp 161-165 °C (lit.); 162-164 °C
UNSPSC 12352100

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