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Thermo Scientific Chemicals
2,3-Dimethoxybenzaldehyde, 98+%
CAS: 86-51-1 | C9H10O3 | 166.176 g/mol
化学物質識別子
CAS86-51-1
IUPAC Name2,3-dimethoxybenzaldehyde
Molecular FormulaC9H10O3
InChI KeyJIVGSHFYXPRRSZ-UHFFFAOYSA-N
SMILESCOC1=CC=CC(C=O)=C1OC
さらに表示
仕様
スペックシート
スペックシート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.
Applications
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.
Solubility
Solubility in methanol with almost transparency.
Notes
Air sensitive. Incompatible with oxidizing agents.
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.
Solubility
Solubility in methanol with almost transparency.
Notes
Air sensitive. Incompatible with oxidizing agents.
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.