220433-57-8

Basic information

• Product Name: 4',5,7-trihydroxy-6-(tricarbonyl[(1'',2'',3'',4''-η)-1'',3''-cyclohexadien-5''α-yl]iron(0))flavanone
• Synonyms: 4',5,7-trihydroxy-6-(tricarbonyl[(1'',2'',3'',4''-η)-1'',3''-cyclohexadien-5''α-yl]iron(0))flavanone
• CAS NO: 220433-57-8
• Molecular Weight: 490.249
• Mol File: 220433-57-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4',5,7-trihydroxy-6-(tricarbonyl[(1'',2'',3'',4''-η)-1'',3''-cyclohexadien-5''α-yl]iron(0))flavanone(CAS DataBase Reference)
• NIST Chemistry Reference: 4',5,7-trihydroxy-6-(tricarbonyl[(1'',2'',3'',4''-η)-1'',3''-cyclohexadien-5''α-yl]iron(0))flavanone(220433-57-8)
• EPA Substance Registry System: 4',5,7-trihydroxy-6-(tricarbonyl[(1'',2'',3'',4''-η)-1'',3''-cyclohexadien-5''α-yl]iron(0))flavanone(220433-57-8)

Safety Data

• Hazardous Substances Data: 220433-57-8(Hazardous Substances Data)

Upstream product

• 480-41-1 5,7-Dihydroxy-2-(4-hydroxy-phenyl)-chroman-4-on 

Relevant articles and documents

Attachment of IR-active organometallic probe groups to flavonoid inducers of nod gene expression

Direct reaction of flavanones with electrophilic tricarbonyl[(1,2,3,4,5-η)cyclohexadienyliron(1+) complexes affords organometallic derivatives for use as probes of molecular recognition events during the induction of nodulation genes in Rhizobium leguminosarum. A more selective preparation method has been developed by deprotonation of the flavanone prior to the addition of the cyclohexadienyliron complex.