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Key Documents

Altri documenti

194468

Sigma-Aldrich

3,4-Dimethoxyphenol

97%

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About This Item

Formula condensata:
(CH3O)2C6H3OH
Numero CAS:
2033-89-8
Peso molecolare:
154.16
Beilstein:
1366650
Numero CE:
217-995-4
Numero MDL:
MFCD00008390
Codice UNSPSC:
12352100
ID PubChem:
24851654
NACRES:
NA.22

Saggio

97%

Forma fisica

solid

Punto di fusione

79-82 °C (lit.)

Stringa SMILE

COc1ccc(O)cc1OC

InChI

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

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Categorie correlate

Applicazioni

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

Pittogrammi

Exclamation mark
GHS07

Avvertenze

Warning

Indicazioni di pericolo

H315 - H319 - H335

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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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
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
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
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