84092-46-6

Basic information

• Product Name: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)-3-(3-methyl-2-butenyl)phenyl]-3-[ 4-(methoxymethoxy)phenyl]-
• CAS NO: 84092-46-6
• Molecular Formula: C26H32O8
• Molecular Weight: 472.535
• Mol File: 84092-46-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)-3-(3-methyl-2-butenyl)phenyl]-3-[ 4-(methoxymethoxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)-3-(3-methyl-2-butenyl)phenyl]-3-[ 4-(methoxymethoxy)phenyl]-(84092-46-6)
• EPA Substance Registry System: 2-Propen-1-one, 1-[2-hydroxy-4,6-bis(methoxymethoxy)-3-(3-methyl-2-butenyl)phenyl]-3-[ 4-(methoxymethoxy)phenyl]-(84092-46-6)

Safety Data

• Hazardous Substances Data: 84092-46-6(Hazardous Substances Data)

Upstream product

• 27364-71-2 2',4',6'-trihydroxy-3'-(3-methyl-2-butenyl)acetophenone 
• 870-63-3 prenyl bromide 
• 65490-09-7 2'-hydroxy-4',6'-bis(methoxymethoxy)acetophenone 
• 480-66-0 2,4,6-trihydroxyacetophenone 
• 6515-21-5 4-methoxymethoxy-benzaldehyde 
• 84092-45-5 2',4'-bis(methoxymethoxy)-5'-(3,3-dimethylallyl)-6'-hydroxyacetophenone 

Downstream Products

• 1174035-58-5 (2Z)-4,6-bis(methoxymethoxy)-2-[4-(methoxymethoxy)benzylidene]-7-(3-methylbut-2-en-1-yl)-1-benzofuran-3(2H)-one 
• 112772-82-4 2,4,4',6-tetrahydroxy-3-(3,3-dimethylallyl)chalcone 
• 68682-02-0 5,7-Dihydroxy-2-(4-hydroxy-phenyl)-8-(3-methyl-but-2-enyl)-chroman-4-one 
• 84092-47-7 5,7,4'-trimethoxymethoxy-8-(3,3-dimethylallyl)-flavanone 

Relevant articles and documents

A one-pot synthesis of aurones from substituted acetophenones and benzaldehydes: A concise synthesis of aureusidin

A one-pot synthesis of aurones from substituted acetophenone and benzaldehyde has been developed on the basis of an improved Algar-Flynn-Oyamada reaction. By using this method, several aurones were prepared in three steps from commercial starting materials. The usefulness of this one-pot strategy was confirmed by a synthesis of aureusidin, an inhibitor of iodothyronine deiodinase, in 41% overall yield. In comparison with a two-step synthesis of this product from the same substrates, the one-pot strategy was more effective, giving a higher yield and requiring fewer and simpler operations. Georg Thieme Verlag Stuttgart New York.

Synthesis, biological evaluation of prenylflavonoids as vasorelaxant and neuroprotective agents

A series of prenylflavonoids with multiple hydroxyl groups were synthesized and evaluated for their vasorelaxant activities against rat aorta rings pre-contracted by phenylephrine (PE), as well as their neuroprotective effects against OGD induced PC12 cel