78316-27-5

Basic information

• Product Name: (+/-)-bavachin
• Synonyms: (+/-)-bavachin
• CAS NO: 78316-27-5
• Molecular Weight: 324.376
• Mol File: 78316-27-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (+/-)-bavachin(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-bavachin(78316-27-5)
• EPA Substance Registry System: (+/-)-bavachin(78316-27-5)

Safety Data

• Hazardous Substances Data: 78316-27-5(Hazardous Substances Data)

Upstream product

• 948307-21-9 2-hydroxy-4,4’-dimethoxy methyl ether-5-isopentenyl chalcone 
• 1314539-20-2 2'-prenyloxy-4'-methoxymethoxyacetophenone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 552-41-0 1-(2-hydroxy-4-methoxyphenyl)ethanone 
• 1092462-95-7 4'-methoxy-4-methoxymethoxy-2'-prenyloxychalcone 
• 78316-24-2 7,4'-di(methoxymethoxy)flavan-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 
• 28437-37-8 5-C-prenylresacetophenone 
• 89-84-9 2',4'-dihydroxy-4-acetophenone 
• 952647-84-6 (E)-1-(2-hydroxy-4-(methoxymethoxy)-5-(3-methylbut-2-en-1-yl)phenyl)-3-(4-(methoxymethoxy)phenyl)prop-2-en-1-one 
• 934247-88-8 7,4'-dimethoxymethoxy-6-(3,3-dimethylallyl)-flavanone 
• 115-18-4 2-methyl-3-buten-2-ol 

Downstream Products

• 78316-28-6 4'-hydroxy-2,2-dimethylpyrano<5,6:6,7>flavanone 
• 78316-29-7 4'-hydroxy-2,2-dimethylpyrano<5,6:6,7>flavone 

Relevant articles and documents

Flavonoids as vasorelaxant agents: Synthesis, biological evaluation and quantitative structure activities relationship (QSAR) studies

A series of 2-(2-diethylamino)-ethoxychalcone and 6-prenyl(or its isomers)-flavanones 10a,b and 11a-g were synthesized and evaluated for their vasorelaxant activities against rat aorta rings pretreated with 1 μM phenylephrine (PE). Several compounds showe

Synthesis of four natural prenylflavonoids and their estrogen-like activities

Four prenylflavonoids, bavachin 1, isobavachin 2, 7,4′-dihydroxy-8- prenylflavone 3, and 8-prenylapigenin 4 were synthesized and recognized for possessing estrogen-like activity in MCF-7/BOS cells, as evaluated by an estrogen-screening assay. All compound