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D116009

Sigma-Aldrich

2,3-Dihydroxynaphthalene

98%

Synonym(s):

2,3-Naphthalenediol

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About This Item

Linear Formula:
C10H6(OH)2
CAS Number:
Molecular Weight:
160.17
Beilstein:
742375
EC Number:
MDL number:
UNSPSC Code:
12352100

Assay

98%

mp

161-165 °C (lit.)

SMILES string

Oc1cc2ccccc2cc1O

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

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Application

Reagent for synthesis of aromatic polyamides, crown ethers, W(VI) complexes, and sulfonic acids.

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Description
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Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

347.0 °F

Flash Point(C)

175 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Makromol. Chem., 194, 1595-1595 (1993)
Journal of the American Chemical Society, 115, 7916-7916 (1993)
Tetrahedron Letters, 34, 1287-1287 (1993)
Xiao-ming Lu et al.
Guang pu xue yu guang pu fen xi = Guang pu, 22(1), 36-38 (2003-08-28)
The title organo-molybdate derivatives are synthesized and their IR, 1H NMR spectra have been determined and the relations between the structures and the 1H NMR and IR parameters have been studied. The results indicate that the red shift of the
M Erben-Russ et al.
International journal of radiation biology and related studies in physics, chemistry, and medicine, 52(3), 393-412 (1987-09-01)
Linoleic acid peroxyl radicals (LOO.) can be viewed as model intermediates occurring during lipid peroxidation processes. Formation and reactions of these species were investigated in aqueous alkaline solution using the technique of pulse radiolysis combined with kinetic spectroscopy. Irradiation of

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