D116408
2,7-Dihydroxynaphthalene
97%
Synonym(s):
2,7-Naphthalenediol
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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
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Related Categories
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
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Efficient lactic acid-catalyzed route to naphthopyranopyrimidines under solvent-free conditions
Sadeh FN, et al.
Organic preparations and procedures international, 49, 35-44 (2017)
Elisa Haug-Schifferdecker et al.
The Journal of biological chemistry, 285(22), 16487-16494 (2010-03-31)
Five fungal genomes from the Ascomycota (sac fungi) were found to contain a gene with sequence similarity to a recently discovered small group of bacterial prenyltransferases that catalyze the C-prenylation of aromatic substrates in secondary metabolism. The genes from Aspergillus
The Journal of Organic Chemistry, 58, 7388-7388 (1993)
Alexandru Chichirau et al.
Free radical biology & medicine, 38(3), 344-355 (2005-01-05)
ortho-Hydroxyphenols (catechols) form a common structural unit in naturally occurring antioxidants such as polyphenols. They also show pro-oxidant characteristics which depend on their particular structure. Here we examined the acetylated versions of three catechols and a naphthalenediol for cytotoxicity to
G J Kemperman et al.
Organic letters, 2(18), 2829-2831 (2000-08-31)
[structure: see text] The cephalosporin antibiotic Cefadroxil can be epimerized at the alpha-carbon of its amino acid side chain using pyridoxal as the mediator. By clathration with 2,7-dihydroxynaphthalene, the desired diastereomer can be selectively withdrawn from the equilibrating mixture of
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