4626-22-6

Basic information

• Product Name: DIHYDROFORMONONETIN
• Synonyms: 2,3-Dihydro-7-hydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one
• CAS NO: 4626-22-6
• Molecular Formula: C₁₆H₁₄O₄
• Molecular Weight: 270.28
• Product Categories: Iso-Flavones
• Mol File: 4626-22-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: DIHYDROFORMONONETIN(CAS DataBase Reference)
• NIST Chemistry Reference: DIHYDROFORMONONETIN(4626-22-6)
• EPA Substance Registry System: DIHYDROFORMONONETIN(4626-22-6)

Safety Data

• Hazardous Substances Data: 4626-22-6(Hazardous Substances Data)

Upstream product

• 95307-71-4 1-[2-hydroxy-4-(phenylmethoxy)phenyl]-2-(4-methoxyphenyl)ethanone 
• 10499-15-7 7-benzyloxy-3-(4-methoxyphenyl)-3H-benzopyran-4-one 
• 108-46-3 recorcinol 
• 485-72-3 7-Hydroxy-3-(4-methoxy-phenyl)-chromen-4-on 
• 104-01-8 4-Methoxyphenylacetic acid 
• 97714-83-5 2-hydroxy-4-ethoxymethoxyphenyl α-hydroxymethyl-4-methoxybenzyl ketone 
• 487-49-0 1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone 
• 97714-86-8 7-ethoxymethoxy-4'-methoxyisoflavanone 
• 10499-17-9 3,4-dihydro-7-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran 

Downstream Products

• 1264702-82-0 C₂₀H₂₃NO₄ 
• 1394853-18-9 C₂₃H₂₉NO₄ 
• 1264702-97-7 C₁₉H₂₁NO₄ 
• 1264702-85-3 C₂₀H₂₃NO₄ 
• 1264702-94-4 C₁₈H₁₉NO₄ 
• 1264702-83-1 C₂₀H₂₅NO₄ 
• 1264702-86-4 C₂₀H₂₅NO₄ 
• 1264702-95-5 C₁₈H₂₁NO₄ 
• 1264834-65-2 C₂₀H₂₃NO₃ 
• 1264834-66-3 C₂₀H₂₃NO₃ 
• 1264834-69-6 C₁₈H₁₉NO₃ 
• 1264702-66-0 C₂₁H₂₃NO₃ 
• 1394853-00-9 C₂₄H₂₉NO₃ 
• 1394853-03-2 C₂₀H₂₁NO₃ 

Relevant articles and documents

Induction of targeted osteogenesis with 3-aryl-2H-benzopyrans and 3-aryl-3H-benzopyrans: Novel osteogenic agents

Development of target oriented chemotherapeutics for treatment of chronic diseases have been considered as an important approach in drug development. Following this approach, in our efforts for exploration of new osteogenic leads, substituted 3-aryl-2H-be

HYDROGEN TRANSFER REDUCTION OF ISOFLAVONES

Hydrogen transfer reduction of isoflavones using ammonium formate and palladium charcoal provides an easy access to polyoxyisoflavanones and also to isoflavan-4-ols without the need for protection of the hydroxy groups.Optimized reaction conditions for im

A New General Synthesis of Polyhydroxyisoflavanones

Hydroxyisoflavanones have been conveniently synthesised from hydroxydesoxybenzoins in 47-57 percent overall yields in four steps which could be carried out either continuously or by isolating the products at each stage.