24672-86-4

Basic information

• Product Name: Isobavachin
• Synonyms: 4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-
• CAS NO: 24672-86-4
• Molecular Formula: C₂₀H₂₀O₄
• Molecular Weight: 324.3704
• Mol File: 24672-86-4.mol
• Article Data: 3

Chemical Properties

• Melting Point: 188-189℃
• Appearance: /
• Density: 1.244±0.06 g/cm3 (20 ºC 760 Torr)
• CAS DataBase Reference: Isobavachin(CAS DataBase Reference)
• NIST Chemistry Reference: Isobavachin(24672-86-4)
• EPA Substance Registry System: Isobavachin(24672-86-4)

Safety Data

• Hazardous Substances Data: 24672-86-4(Hazardous Substances Data)

Usage

Uses

(±)-Isobavachin is recognized for possessing estrogen-like activity in MCF-7/BOS cells.

Upstream product

• 115-18-4 2-methyl-3-buten-2-ol 
• 69097-97-8 7,4'-dihydroxy-dihydroflavone 
• 948307-22-0 7,4'-dimethoxymethoxy-8-(3,3-dimethylallyl)-flavanone 
• 1134396-40-9 8-allyl-7-(methoxymethoxy)-2-(4-(methoxymethoxy)phenyl)chroman-4-one 
• 124775-22-0 1-<2-Hydroxy-4-(methoxymethoxy)phenyl>-3-<4-(methoxymethoxy)phenyl>prop-2-en-1-on 
• 65490-08-6 2-hydroxy-4-(methoxymethoxy)acetophenone 
• 870-63-3 prenyl bromide 
• 54730-26-6 4-methoxymethoxy-3-(3,3-dimethylallyl)-2-hydroxyacetophenone 
• 19825-40-2 2,4-Dihydroxy-3-C-prenylacetophenone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 

Downstream Products

• 78332-22-6 4'-hydroxy-2,2-dimethylpyrano<5,6:8,7>flavone 
• 78316-30-0 4'-hydroxy-2,2-dimethylpyrano<5,6:8,7>flavanone 

Relevant articles and documents

8-Prenylflavanones through Microwave Promoted Tandem Claisen Rearrangement/6-endo-trig Cyclization and Cross Metathesis

Prenylated flavanones were obtained from ortho-allyloxy chalcones through a one-pot sequence of Claisen rearrangement and 6-endo-trig cyclization, followed by olefin cross metathesis of the intermediate allyl flavanones with 2-methyl-2-butene. The synthet

New Syntheses of 4',7-Dihydroxy-6,8-di-C-prenylflavanone, Bavachin, Isobavachin and Related Compounds

The titel compounds have been synthesised by nuclear prenylation of 4',7-dihydroxyflavanone(liquiritigenin, III), Cyclodehydrogenation of bavachin and isobavachin with DDQ yields the chromenoflavanones (VIII) and (X) respectively which on dehydrogenation