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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


Certificados de análisis (COA)

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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
M N M Cunha et al.
Colloids and surfaces. B, Biointerfaces, 154, 210-220 (2017-03-28)
Silver nanoparticles (AgNPs) were synthesized by citrate reduction method in the presence of polymers, poly(ethylene glycol) (PEG), poly(vinyl alcohol) (PVA) and chitosan, used as stabilizing agents, and an oxidoreductase enzyme, laccase (Lac), with the goal of expanding the NPs antimicrobial
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
H Takii et al.
Bioscience, biotechnology, and biochemistry, 61(9), 1531-1535 (1997-10-27)
Glycosides were screened for their lowering effect on the postprandial blood glucose rise in vivo. The effect of phlorizin and other phenolic glycosides on the postprandial blood glucose response to glucose ingestion was evaluated in Std ddY mice. When phlorizin
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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