1229515-77-8

Basic information

• Product Name: (2E)-1-[3-geranyl-2-hydroxy-4-(methoxymethoxy)phenyl]-3-{4-{[2-(trimethylsilyl)ethoxy]methoxy}-phenyl}prop-2-en-1-one
• Synonyms: (2E)-1-[3-geranyl-2-hydroxy-4-(methoxymethoxy)phenyl]-3-{4-{[2-(trimethylsilyl)ethoxy]methoxy}-phenyl}prop-2-en-1-one
• CAS NO: 1229515-77-8
• Molecular Weight: 566.81
• Mol File: 1229515-77-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2E)-1-[3-geranyl-2-hydroxy-4-(methoxymethoxy)phenyl]-3-{4-{[2-(trimethylsilyl)ethoxy]methoxy}-phenyl}prop-2-en-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-1-[3-geranyl-2-hydroxy-4-(methoxymethoxy)phenyl]-3-{4-{[2-(trimethylsilyl)ethoxy]methoxy}-phenyl}prop-2-en-1-one(1229515-77-8)
• EPA Substance Registry System: (2E)-1-[3-geranyl-2-hydroxy-4-(methoxymethoxy)phenyl]-3-{4-{[2-(trimethylsilyl)ethoxy]methoxy}-phenyl}prop-2-en-1-one(1229515-77-8)

Safety Data

• Hazardous Substances Data: 1229515-77-8(Hazardous Substances Data)

Upstream product

• 1219966-99-0 1-{3-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2-hydroxy-4-(methoxymethoxy)phenyl}ethanone 

Downstream Products

• 1229515-79-0 8-[(2E)-3,7-dimethylocta-2,6-dien-1-yl]-2,3-dihydro-7-(methoxymethoxy)-2-{4-{[2-(trimethylsilyl)-ethoxy]methoxy}phenyl}-4H-1-benzopyran-4-one 
• 62949-76-2 xanthoangelol 

Relevant articles and documents

New synthetic routes to biologically interesting geranylated flavanones and geranylated chalcones: First total synthesis of (±)-prostratol F, xanthoangelol, and (±)-lespeol

A new and efficient synthetic approach to biologically interesting geranylated flavanones and geranylated chalcones is described. Thus, the first total syntheses of the geranylated flavanones (±)-prostratol F (1), (±)-8-geranyl-3′,4′,7-trihydroxyflavanone (2), and (±)-6-geranyl-5,7-dihydroxy-3′,4′-dimethoxyflavanone (3) were carried out starting from 2,4-dihydroxyacetophenone (10) and 2,4,6-trihydroxyacethophenone (17) in five to six steps (Schemes 2 and 3). The geranylated chalcones xanthoangelol (4), 3-geranyl-2,3′,4,4′- tetrahydroxychalcone (5), (±)-lespeol (6), and lespeol derivatives (±)-7-9 were synthesized starting from 2,4-dihydroxyacetophenone (10) in three to four steps (Schemes 2 and 6).