37760
2,3-Dihydroxynaphthalene
≥98.0% (HPLC)
Synonyme(s) :
2,3-Naphthalenediol
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About This Item
Formule linéaire :
C10H6(OH)2
Numéro CAS:
Poids moléculaire :
160.17
Numéro Beilstein :
742375
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
≥98.0% (HPLC)
Résidus de sublimation
≤1%
Pf
161-165 °C (lit.)
162-164 °C
Chaîne SMILES
Oc1cc2ccccc2cc1O
InChI
1S/C10H8O2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,11-12H
Clé InChI
JRNGUTKWMSBIBF-UHFFFAOYSA-N
Informations sur le gène
human ... BAD(572)
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Catégories apparentées
Description générale
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.
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
Mention d'avertissement
Danger
Mentions de danger
Conseils de prudence
Classification des risques
Acute Tox. 4 Oral - Eye Dam. 1
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
347.0 °F
Point d'éclair (°C)
175 °C
Équipement de protection individuelle
dust mask type N95 (US), Eyeshields, Gloves
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Les clients ont également consulté
Application of cyclophosphazene derivatives as flame retardants for ABS.
Shin YJ, et al.
Journal of Industrial and Engineering Chemistry (Amsterdam, Netherlands), 16(3), 364-367 (2010)
Chemical speciation of iron in seawater by cathodic stripping voltammetry with dihydroxynaphthalene.
Constant M G van den Berg
Analytical chemistry, 78(1), 156-163 (2005-12-31)
The chemical speciation of iron in seawater is determined by cathodic stripping voltammetry using 2,3-dihydroxynaphthalene (DHN) as adsorptive and competing ligand. The optimized conditions include a DHN concentration of 0.5-1 microM, seawater at its original pH of 8, and equilibration
Kentaro Nakanishi et al.
The Journal of organic chemistry, 79(6), 2625-2631 (2014-02-26)
The construction of dinaphtho[2,1-b;2',3'-d]furan-6-ol was developed via a dehydration reaction involving two molecules of 2,3-dihydroxynaphthalene in the presence of a strong acid. Starting from the dinaphthofuran, a variety of butterfly shaped derivatives were synthesized. The optical properties of these compounds
Tatjana D Savić et al.
Nanoscale, 4(5), 1612-1619 (2012-02-09)
Surface modification of nanocrystalline TiO(2) particles (45 Å) with catecholate-type ligands consisting of an extended aromatic ring system, i.e., 2,3-dihydroxynaphthalene and anthrarobin, was found to alter the optical properties of the nanoparticles in a similar way to modification with catechol.
Synthesis of bis (ether anhydride) s for poly (ether imide) s having 1, 2-linked units by nitrodisplacement with catechol derivatives.
Eastmond GC and Paprotny J.
Macromolecules, 28(7), 2140-2146 (1995)
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