56252-02-9

Basic information

• Product Name: Hydroxyanigorufone
• Synonyms: Hydroxyanigorufone;2-Hydroxy-9-(4-hydroxyphenyl)-1H-phenalen-1-one;Emenolone
• CAS NO: 56252-02-9
• Molecular Formula: C₁₉H₁₂O₃
• Molecular Weight: 288.29678
• Mol File: 56252-02-9.mol
• Article Data: 3

Chemical Properties

• Melting Point: 201-204℃
• Appearance: /
• CAS DataBase Reference: Hydroxyanigorufone(CAS DataBase Reference)
• NIST Chemistry Reference: Hydroxyanigorufone(56252-02-9)
• EPA Substance Registry System: Hydroxyanigorufone(56252-02-9)

Safety Data

• Hazardous Substances Data: 56252-02-9(Hazardous Substances Data)

Upstream product

• 7400-08-0 p-Coumaric Acid 
• 66-77-3 1-naphthaldehyde 
• 98978-43-9 (E)-ethyl 3-(naphthalen-1-yl)acrylate 
• 13026-12-5 (E)-3-(naphthalen-1-yl)acrylic acid 
• 120681-10-9 (E)‐3‐(naphthalen‐1‐yl)acryloyl chloride 
• 548-39-0 Perinaphthenon 
• 65874-43-3 9-(4-methoxyphenyl)-1H-phenalen-1-one 
• 13139-86-1 4-methoxyphenyl magnesium bromide 
• 65874-44-4 2-hydroxy-9-(4'-methoxyphenyl)-1H-phenalen-1-one 

Downstream Products

• 56252-06-3 2-methoxy-9-(4'-methoxyphenyl)phenalen-1-one 

Relevant articles and documents

Intermediates With Biosynthetic Implications In De Novo Production Of Phenyl-Phenalenone-Type Phytoalexins By Musa acuminata Revised Structure Of Emenolone

Three new intermediates (1-3) in de novo biosynthetic pathway to phenyl-phenalenone-type phytoalexins have been isolated from rhizomes of Musa acuminata infected with the fungus Fusarium oxysporum.The structures of the new pre-phytoalexins were elucidated

Variability of phenylpropanoid precursors in the biosynthesis of phenylphenalenones in Anigozanthos preissii

Feeding experiments using 13C labelled precursors and NMR spectroscopic studies revealed general biosynthetic incorporation of phenylalanine and variable incorporation of cinnamic acid, p-coumaric acid, caffeic acid and ferulic acid into phenylphenalenones in root cultures of Anigozanthos preissii. Evidence was obtained for parallel pathways of phenylphenalenone biosynthesis, with respect to the left phenylpropanoid unit, and a sequence involving utilisation of p-coumaric acid with late generation of an intermediate catechol moiety in the right phenylpropanoid unit. (C) 2000 Elsevier Science Ltd.