129097-15-0

Basic information

• Product Name: 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one
• Synonyms: 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one
• CAS NO: 129097-15-0
• Molecular Weight: 338.403
• Mol File: 129097-15-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one(129097-15-0)
• EPA Substance Registry System: 2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-en-1-yl)chroman-4-one(129097-15-0)

Safety Data

• Hazardous Substances Data: 129097-15-0(Hazardous Substances Data)

Upstream product

• 128961-19-3 7-methoxy-2-(4-(methoxymethoxy)phenyl)-6-(3-methylbut-2-en-1-yl)chroman-4-one 
• 123-08-0 4-hydroxy-benzaldehyde 
• 128961-13-7 (E)-1-(2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl)-3-(4-(methoxymethoxy)phenyl)prop-2-en-1-one 
• 128961-25-1 1-(4-methoxy-2-((3-methylbut-2-en-1-yl)oxy)phenyl)ethan-1-one 
• 28448-83-1 2′-hydroxyl-4′-methoxyl-5′-isopentenylacetophenone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 20784-60-5 (E)-1-(2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 

Downstream Products

• 19879-30-2 (R)-bavachinin 
• 19879-30-2 -(2-hydroxy-3-methylbutane)-2-(4-hydroxyphenyl)-7-methoxychroman-4-one 

Relevant articles and documents

Separation and peroxisome proliferator-activated receptor-γ agonist activity evaluation of synthetic racemic bavachinin enantiomers

Abstract Bavachinin, isolated from Psoralea corylifolia seeds, has been reported to demonstrate peroxisome proliferator-activated receptor-γ (PPAR-γ) agonist activity. However, isolated bavachinin is actually a mixture of S and R configurations, with an e

Synthesis method of active component of Chinese herb psoralea corylifolia

The invention relates to a synthesis method of an active component of a Chinese herb psoralea corylifolia. The synthesis method comprises the following steps: (a), mixing paeonol, 1-bromo-3-methyl-2-butene and acetone, adding potassium carbonate, and then

An Improved Procedure for Cyclisation of Chalcones to Flavanones Using Celite Supported Potassium Fluoride in Methanol: Total Synthesis of Bavachinin

Chalcones may be cyclised to the corresponding flavanones by stirring with KF - celite suspended in methanol at reflux.This method gives consistently higher conversion than other reported procedures and its utility is illustrated by the synthesis of the l