2,3-Dimetoxibenzaldehído, +98 %, Thermo Scientific Chemicals

CAS: 86-51-1 | C9H10O3 | 166.176 g/mol

Número de catálogo	Cantidad
A14080.14 también denominado A14080-14	25 g

Número de catálogo A14080.14

también denominado A14080-14

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Identificadores químicos

CAS86-51-1

IUPAC Name2,3-dimethoxybenzaldehyde

Molecular FormulaC9H10O3

InChI KeyJIVGSHFYXPRRSZ-UHFFFAOYSA-N

SMILESCOC1=CC=CC(C=O)=C1OC

Especificaciones Specification Sheet

Appearance (Color)White to pale cream

FormCrystals or powder or crystalline powder or lumps or chunks

Assay (GC)≥98.0%

Free acid (titration)≤1%

Melting Point (clear melt)48.0-54.0?C

2,3-Dimethoxybenzaldehyde possess antifungal activity of redox-active benzaldehydes that target cellular antioxidation. It could function as chemosensitizing agents in concert with conventional drugs to improve antifungal efficacy.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Aplicaciones
El 2,3-dimetoxibenzaldehído posee actividad antifúngica de benzaldehídos redox activos que tienen por objetivo la antioxidación celular. Podría funcionar como agente quimiosensibilizante en combinación con fármacos convencionales para mejorar la eficacia antifúngica.

Solubilidad
Solubilidad en metanol casi transparente.

Notas
Sensible al aire. Incompatible con agentes oxidantes.

RUO – Research Use Only

General References:

W.David Ollis; Brian T.Redman; Richard J.Roberts; Ian O.Sutherland; Otto R.Gottlieb; Mauro T.Magalhaaes. Neoflavonoids and the cinnamylphenol kuhlmannistyrene from Machaerium kuhlmannii and M. Nictitans. Phytochemistry. 1978, 17,(8), 1383-1388.
K.Orito; R.H.Manske; R.Rodrigo. Photosensitized oxidation of an enaminoketone. Total synthesis of a rhoeadine alkaloid. J. Am. Chem. Soc. 1974, 96,(6), 1944-1945.