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Merck
CN

37765

2,6-二羟基萘

purum, ≥96.0% (HPLC)

别名:

2,6-萘二酚

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线性分子式:
C10H6(OH)2
化学文摘社编号:
分子量:
160.17
EC Number:
209-465-6
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1238082
MDL number:
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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.)

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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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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