28448-83-1

Basic information

• Product Name: Ethanone, 1-[2-hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-
• CAS NO: 28448-83-1
• Molecular Formula: C14H18O3
• Molecular Weight: 234.295
• Mol File: 28448-83-1.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-(28448-83-1)
• EPA Substance Registry System: Ethanone, 1-[2-hydroxy-4-methoxy-5-(3-methyl-2-butenyl)phenyl]-(28448-83-1)

Safety Data

• Hazardous Substances Data: 28448-83-1(Hazardous Substances Data)

Upstream product

• 870-63-3 prenyl bromide 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 128961-25-1 1-(4-methoxy-2-((3-methylbut-2-en-1-yl)oxy)phenyl)ethan-1-one 
• 28437-37-8 5-C-prenylresacetophenone 
• 77-78-1 dimethyl sulfate 
• 87080-11-3 2,4-Dimethoxy-5-C-prenylacetophenone 

Downstream Products

• 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 
• 1348361-30-7 3-(4-hydroxyphenyl)-6-isopentenyl-7-methoxy-4H-chromen-4-one 
• 52679-14-8 2'-hydroxyl-4'-methoxy-5'-prenylchalcone 

Relevant articles and documents

2-phenylchroman-4-one derivatives and antiviral composition comprising the same

The present invention relates to a 2-phenylchroman-4-one derivative or a pharmaceutically acceptable salt thereof, a method for manufacturing the same, and a therapeutic agent for MERS containing the same as an active component. A compound containing the

Bavachinin analogues as agonists of pan-peroxisome proliferator-activated receptors

Peroxisome proliferator-activated receptors (PPARs) agonists contribute to the regulation of glucose, lipid, and cholesterol metabolism and have emerged as key targets to treat metabolic syndrome. In our previous study, the natural compound bavachinin was found to have pan-PPAR agonist activity. In this study, five isoflavones, three isoflavanones, and five scaffold-hopping analogues of bavachinin were designed, synthesised, and evaluated through reporter gene assays for pan-PPAR agonist activity. The analogue 2-(4-hydroxyphenyl)-6-isopentenyl-7-methoxy-2,3-dihydroquinolin-4(1H)-one (21) was identified as a pan-PPAR agonist, exhibiting substantially higher PPAR α/β agonist activity and equal PPAR-γ agonist activity than does bavachinin.

Method for synthesizing active ingredient intermediate of traditional Chinese medicine fructus psoraleae

The invention relates to a method for synthesizing an active ingredient intermediate of a traditional Chinese medicine fructus psoraleae. The method comprises the following steps: (a) mixing paeonol,1-bromo-3-methyl-2-butene and acetone, and adding potass