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Thermo Scientific Chemicals
3,4,5-Trimethoxyphenol, 97%
CAS: 642-71-7 | C9H12O4 | 184.191 g/mol
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Catalog number L01527.14
also known as L01527-14
Price (EUR)
250,00
Each
Quantity:
25 g
Price (EUR)
250,00
Each
Chemical Identifiers
CAS642-71-7
IUPAC Name3,4,5-trimethoxyphenol
Molecular FormulaC9H12O4
InChI KeyVTCDZPUMZAZMSB-UHFFFAOYSA-N
SMILESCOC1=CC(O)=CC(OC)=C1OC
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream to yellow to brown
FormPowder
Assay (GC)≥96.0%
Identification (FTIR)Conforms
Melting Point (clear melt)142-149?C
3,4,5-Trimethoxyphenol is used as Flavonoid drug intermediates. It is used for pharmaceutical, cosmetics, agrochemicals and food industry research.
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
3,4,5-Trimethoxyphenol is used as Flavonoid drug intermediates. It is used for pharmaceutical, cosmetics, agrochemicals and food industry research.
Solubility
Soluble in chloroform.
Notes
Light Sensitive. Store in the dark. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
3,4,5-Trimethoxyphenol is used as Flavonoid drug intermediates. It is used for pharmaceutical, cosmetics, agrochemicals and food industry research.
Solubility
Soluble in chloroform.
Notes
Light Sensitive. Store in the dark. Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
RUO – Research Use Only
General References:
- M. Agostinha R. Matosa; Margarida S. Mirandaa; Victor M.F. Morais. 3,4,5-Trimethoxyphenol: A combined experimental and theoretical thermochemical investigation of its antioxidant capacity.The Journal of Chemical Thermodynamics.2008, 40 625-631.
- Fokas Demosthenes; Hamzik James A. One-Pot Synthesis of 7-Aryl-Octahydroazonino[5,4-b]indoles Based on the Fragmentation of Indolizino[8,7-b]indoles and the Insertion of Indoles and 3,4,5-Trimethoxyphenol..Synlett.2009, 4 581-584.