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Merck

194468

Sigma-Aldrich

3,4-Dimethoxyphenol

97%

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About This Item

Fórmula lineal:
(CH3O)2C6H3OH
Número de CAS:
Peso molecular:
154.16
Beilstein/REAXYS Number:
1366650
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

97%

form

solid

mp

79-82 °C (lit.)

SMILES string

COc1ccc(O)cc1OC

InChI

1S/C8H10O3/c1-10-7-4-3-6(9)5-8(7)11-2/h3-5,9H,1-2H3

InChI key

SMFFZOQLHYIRDA-UHFFFAOYSA-N

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Application

3,4-Dimethoxyphenol was used in the synthesis of:
  • 5,6-dimethoxy benzofuranone derivatives, multi-target anti Alzheimer compounds
  • 3,4-dimethoxyphenyl-β-D-glucopyranoside
  • 4-(but-2-enyloxy)-1,2-dimethoxybenzene
  • precursors for the synthesis of the 4H-chromenes

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Hamid Nadri et al.
Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences, 21(1), 15-15 (2013-03-01)
Several studies have been focused on design and synthesis of multi-target anti Alzheimer compounds. Utilizing of the dual Acetylcholinesterase/Butyrylcholinesterase inhibitors has gained more interest to treat the Alzheimer's disease. As a part of a research program to find a novel
Peter Lorenz et al.
Chemistry & biodiversity, 15(5), e1800035-e1800035 (2018-03-27)
Seeds from Hypericum species have recently been identified as an interesting source of xanthone derivatives. Extraction of seeds from H. perforatum with MeOH and subsequent concentration via polyamide adsorption yielded a fraction enriched in tetrahydroxyxanthones (THX), which were further semipurified
Ring-closing metathesis for the synthesis of 2H-and 4H-chromenes.
van Otterlo WAL, et al.
Tetrahedron, 61(42), 9996-10006 (2005)
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