1,2,3-Tri-O-methyl-7,8-O,O-methyleneflavellagic acid

95%

Reagent Code: #241333
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CAS Number 69251-99-6

science Other reagents with same CAS 69251-99-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.283 g/mol
Formula C₁₈H₁₂O₉
thermostat Physical Properties
Boiling Point 649.8±55.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.6±0.1g/ml
Storage 2-8℃

description Product Description

Used in research as a methylated derivative of flavellagic acid, this compound serves as a reference standard in phytochemical studies, particularly in the analysis of tannins and ellagitannin metabolites. Its modified structure enhances stability and solubility, making it suitable for chromatographic and mass spectrometric applications. It is also employed in metabolic pathway investigations to trace the transformation of polyphenolic compounds in biological systems. Due to the methylenedioxy and methyl group protections, it aids in structure-activity relationship studies of antioxidant and enzyme-inhibiting natural products.

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inventory 5mg
10-20 days ฿31,460.00

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1,2,3-Tri-O-methyl-7,8-O,O-methyleneflavellagic acid
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Used in research as a methylated derivative of flavellagic acid, this compound serves as a reference standard in phytochemical studies, particularly in the analysis of tannins and ellagitannin metabolites. Its modified structure enhances stability and solubility, making it suitable for chromatographic and mass spectrometric applications. It is also employed in metabolic pathway investigations to trace the transformation of polyphenolic compounds in biological systems. Due to the methylenedioxy and methyl

Used in research as a methylated derivative of flavellagic acid, this compound serves as a reference standard in phytochemical studies, particularly in the analysis of tannins and ellagitannin metabolites. Its modified structure enhances stability and solubility, making it suitable for chromatographic and mass spectrometric applications. It is also employed in metabolic pathway investigations to trace the transformation of polyphenolic compounds in biological systems. Due to the methylenedioxy and methyl group protections, it aids in structure-activity relationship studies of antioxidant and enzyme-inhibiting natural products.

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