13186-08-8

Basic information

• Product Name: 7,4'-Di-O-methyltectorigenin
• Synonyms: 3-(4-Methoxyphenyl)-5-hydroxy-6,7-dimethoxy-4H-1-benzopyran-4-one;5-Hydroxy-4',6,7-trimethoxyisoflavone;7,4'-Dimethyltectorigenin;7,4'-Di-O-methyltectorigenin
• CAS NO: 13186-08-8
• Molecular Formula: C₁₈H₁₆O₆
• Molecular Weight: 328.32
• Mol File: 13186-08-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 7,4'-Di-O-methyltectorigenin(CAS DataBase Reference)
• NIST Chemistry Reference: 7,4'-Di-O-methyltectorigenin(13186-08-8)
• EPA Substance Registry System: 7,4'-Di-O-methyltectorigenin(13186-08-8)

Safety Data

• Hazardous Substances Data: 13186-08-8(Hazardous Substances Data)

Upstream product

• 2345-17-7 4'-methoxytectorigenin 
• 77-78-1 dimethyl sulfate 
• 491-80-5 5,7-Dihydroxy-3-(4-methoxy-phenyl)-chromen-4-on 
• 124-41-4 sodium methylate 
• 34086-51-6 4',7-dimethoxy-5-hydroxyisoflavone 
• 104-47-2 p-methoxybenzylnitrile 
• 22110-04-9 6-hydroxy-2,3,4-trimethoxyphenyl p-methoxybenzyl ketone 
• 13077-75-3 2,3-dimethoxy-1,6-dihydroxybenzene 
• 857564-82-0 1-(2',6'-dihydroxy-3',4'-dimethoxyphenyl)-2-(4''-methoxyphenyl)ethanone 
• 109-94-4 formic acid ethyl ester 
• 4755-77-5 Ethyl oxalyl chloride 
• 4332-73-4 4',5,6,7-tetramethoxyisoflavone 
• 135010-75-2 7-methoxy-5,6,4'-trihydroxyisoflavone 
• 74-88-4 methyl iodide 

Downstream Products

• 14560-51-1 5-acetoxy-6,7-dimethoxy-3-(4-methoxy-phenyl)-chromen-4-one 
• 857564-82-0 1-(2',6'-dihydroxy-3',4'-dimethoxyphenyl)-2-(4''-methoxyphenyl)ethanone 
• 13539-24-7 5-hydroxy-7,8-dimethoxy-3-(4'-methoxyphenyl)-4H-1-benzopyran-4-one 
• 13539-26-9 6-Hydroxygenistein 

Relevant articles and documents

Synthesis and single crystal X-ray structure of [Na(H2O) 2(C18H15O6SO3)] 2

[Na(H2O)2(C18H15O 6SO3)]2 was synthesized by sulfated 5-hydroxy-6,7,4′-trimethoxyisoflavone with concentrated sulfuric acid. Single-crystal X-ray diffraction study indicates that

Chalcone analog as well as preparation method and use thereof

The invention discloses a chalcone analog represented by a formula (I) as well as a preparation method and use of the chalcone analog. A pharmacodynamic test proves that the compound, namely the chalcone analog, has a good anti-tumor effect.