D116408
2,7-Dihydroxynaphthalene
97%
Synonym(s):
2,7-Naphthalenediol
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
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
Looking for similar products? Visit Product Comparison Guide
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.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Efficient lactic acid-catalyzed route to naphthopyranopyrimidines under solvent-free conditions
Organic preparations and procedures international, 49, 35-44 (2017)
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
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
J. Chem. Soc. Perkin Trans. II, 721-721 (1993)
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service