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About This Item
Linear Formula:
C10H6(OH)2
CAS Number:
Molecular Weight:
160.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-478-7
Beilstein/REAXYS Number:
2042383
MDL number:
Assay:
97%
Form:
powder
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
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.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| D116408-100G | 04061835556434 |
| D116408-5G | 04061835556441 |
