194468
3,4-Dimethoxyphenol
97%
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About This Item
Linear Formula:
(CH3O)2C6H3OH
CAS Number:
Molecular Weight:
154.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-995-4
Beilstein/REAXYS Number:
1366650
MDL number:
Assay:
97%
Form:
solid
Quality Level
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
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
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 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Ring-closing metathesis for the synthesis of 2H-and 4H-chromenes.
van Otterlo WAL, et al.
Tetrahedron, 61(42), 9996-10006 (2005)
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 194468-10G | 04061838761279 |