All Photos(2)
Synonym(s):
2,7-Naphthalenediol
Linear Formula:
C10H6(OH)2
CAS Number:
Molecular Weight:
160.17
Beilstein:
2042383
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
97%
form
powder
mp
185-190 °C (lit.)
SMILES string
Oc1ccc2ccc(O)cc2c1
InChI
1S/C10H8O2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/h1-6,11-12H
InChI key
DFQICHCWIIJABH-UHFFFAOYSA-N
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General description
2,7-Dihydroxynaphthalene is a organic building block used to prepare sulfonic acids, divinylnaphthalenes, dyes, pigments, and fluorescent whiteners.
Application
Starting material for the synthesis of sulfonic acids and divinylnaphthalenes.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 2
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Raafat M Issa et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 62(4-5), 980-986 (2005-06-14)
The absorption spectra of mono- and bis-azo-derivatives obtained by coupling the diazonium salts of aromatic amines and 2,7-dihydroxynaphthalene have been studied in six organic solvents. The different absorption bands have been assigned and the effect of solvents on the charge
C R Bloom et al.
Biochemistry, 36(42), 12746-12758 (1997-10-23)
The binding of phenolic ligands to the insulin hexamer occurs as a cooperative allosteric process. Investigations of the allosteric mechanism from this laboratory resulted in the postulation of a model consisting of a three-state conformational equilibrium and the derivation of
Adriana Trapani et al.
Carbohydrate polymers, 207, 720-728 (2019-01-03)
The antibacterial activity of the S-unsubstituted- and S-benzyl-substituted-2-mercapto-benzothiazoles 1-4 has been evaluated after complexation with Methyl-β-Cyclodextrin (Me-β-CD) or incorporation in solid dispersions based on Pluronic® F-127 and compared with that of the pure compounds. This with the aim to gain
Allergic contact dermatitis from 2,7-dihydroxynaphthalene in hair dye.
A Eskelinen et al.
Contact dermatitis, 36(6), 312-313 (1997-06-01)
Efficient lactic acid-catalyzed route to naphthopyranopyrimidines under solvent-free conditions
Sadeh FN, et al.
Organic preparations and procedures international, 49, 35-44 (2017)
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