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V800014
2-Naphthol
≥98%, solid, Vetec™, LR grade
Synonym(e):
β-Naphthol, 2-Hydroxynaphthalin
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Über diesen Artikel
Lineare Formel:
C10H7OH
CAS-Nummer:
Molekulargewicht:
144.17
UNSPSC Code:
12352300
PubChem Substance ID:
EC Number:
205-182-7
Beilstein/REAXYS Number:
742134
MDL number:
Assay:
≥98%
Form:
solid
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Unterstützung erhaltenProduktname
2-Naphthol, LR, ≥98%
grade
LR
vapor density
4.97 (vs air)
vapor pressure
10 mmHg ( 145.5 °C)
product line
Vetec™
assay
≥98%
form
solid
bp
285-286 °C (lit.)
mp
120-122 °C (lit.)
SMILES string
Oc1ccc2ccccc2c1
InChI
1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
InChI key
JWAZRIHNYRIHIV-UHFFFAOYSA-N
Legal Information
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
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signalword
Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Eye Dam. 1 - Skin Sens. 1
Lagerklasse
11 - Combustible Solids
wgk
WGK 2
flash_point_f
307.4 °F - closed cup
flash_point_c
153 °C - closed cup
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Verwandter Inhalt
Glenn Talaska et al.
Toxicology letters, 213(1), 45-48 (2011-05-26)
Urinary bladder cancer is a historical disease of rubber workers often been associated with exposure to aromatic amines such as 2-naphthylamine. While exposure to these compounds has decreased markedly over time, the bladder cancer risk has not decreased in direct
Supriti Sen et al.
The Analyst, 137(17), 3975-3981 (2012-07-13)
An efficient water soluble fluorescent Al(3+) receptor, 1-[[(2-furanylmethyl)imino]methyl]-2-naphthol (1-H) was synthesized and characterized by physico-chemical and spectroscopic tools along with single crystal X-ray crystallography. High selectivity and affinity of 1-H towards Al(3+) in HEPES buffer (DMSO/water: 1/100) of pH 7.4
Erin E Podlesny et al.
Organic letters, 14(6), 1408-1411 (2012-03-01)
The first enantioselective total synthesis of the bisanthraquinone (S)-bisoranjidiol and an unnatural regioisomer has been accomplished. Key features of the synthesis include the asymmetric oxidative biaryl coupling of a hindered 8-substituted 2-naphthol, selective para-quinone formation, and regioselective tandem Diels-Alder/aromatization reactions.