37765
2,6-Dihydroxynaphthalene
purum, ≥96.0% (HPLC)
Synonym(s):
2,6-Naphthalenediol
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About This Item
Linear Formula:
C10H6(OH)2
CAS Number:
Molecular Weight:
160.17
EC Number:
209-465-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1238082
MDL number:
InChI key
MNZMMCVIXORAQL-UHFFFAOYSA-N
InChI
1S/C10H8O2/c11-9-3-1-7-5-10(12)4-2-8(7)6-9/h1-6,11-12H
SMILES string
Oc1ccc2cc(O)ccc2c1
grade
purum
assay
≥96.0% (HPLC)
mp
220-224 °C, 223-225 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
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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Alberto Macone et al.
Bioorganic & medicinal chemistry, 17(16), 6003-6007 (2009-07-21)
Aromatic substrates tyrosol (p-hydroxyphenylethanol) and 2,6-dihydroxynaphthalene (2,6-DHN) were converted into chromane derivatives by means of chemoenzymatic reactions catalyzed by the aromatic prenyltransferase of bacterial origin NovQ, using dimethylallyl bromide as allylic substrate instead of the natural isoprenyl pyrophosphate substrate. Stereoselective
Mårten Jacobsson et al.
Journal of medicinal chemistry, 49(6), 1932-1938 (2006-03-17)
The antiproliferative activity of the 14 isomeric monoxylosylated dihydroxynaphthalenes has been tested in vitro toward normal HFL-1 and 3T3 A31 cells as well as transformed T24 and 3T3 SV40 cells. The antiproliferative effect toward HFL-1 cells was correlated with the
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