137790-51-3

Basic information

• Product Name: Ethanone, 1-[2-(benzoyloxy)-4,6-bis(phenylmethoxy)phenyl]-
• CAS NO: 137790-51-3
• Molecular Formula: C29H24O5
• Molecular Weight: 452.507
• Mol File: 137790-51-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-(benzoyloxy)-4,6-bis(phenylmethoxy)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-(benzoyloxy)-4,6-bis(phenylmethoxy)phenyl]-(137790-51-3)
• EPA Substance Registry System: Ethanone, 1-[2-(benzoyloxy)-4,6-bis(phenylmethoxy)phenyl]-(137790-51-3)

Safety Data

• Hazardous Substances Data: 137790-51-3(Hazardous Substances Data)

Usage

General Description

Ethanone, 1-[2-(benzoyloxy)-4,6-bis(phenylmethoxy)phenyl]- is a complex chemical compound that contains multiple benzoyloxy and phenylmethoxy groups attached to a central phenyl ring. Ethanone, 1-[2-(benzoyloxy)-4,6-bis(phenylmethoxy)phenyl]- is likely a synthetic derivative with potential applications in the fields of organic chemistry, pharmaceuticals, or materials science due to its intricate structure and potential reactivity. Further research may be needed to fully understand the properties and potential uses of this unique chemical compound.

Upstream product

• 18065-05-9 1-[2,4-bis(benzyloxy)-6-hydroxyphenyl]ethanone 
• 98-88-4 benzoyl chloride 
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• 480-40-0 5,7-dihydroxy-2-phenyl-chromen-4-one 
• 100-39-0 benzyl bromide 
• 65-85-0 benzoic acid 
• 480-66-0 2,4,6-trihydroxyacetophenone 
• 108-73-6 3,5-dihydroxyphenol 

Downstream Products

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• 548-83-4 galangin 
• 110506-85-9 7-(benzyloxy)-5-hydroxy-2-phenyl-4H-chromen-4-one 

Relevant articles and documents

Synthesis and Biological Evaluation of 4-Substituted Kaempfer-3-ols

The synthesis of two series of five kaempfer-3-ols was described. The first set all have a C-3 hydroxyl group and the second has a carboxymethoxy ether at the C-3 position. Both series have variable substitution at the C-4 position (i.e., OH, Cl, F, H, OMe). Both kaempferols and carboxymethoxy ethers were evaluated for their ability to inhibit ribosomal s6 kinase (RSK) activity and cancer cell proliferation.

Isotopic labelling of quercetin 3-glucoside

The potentially important dietary antioxidant, quercetin 3-O-β-d-glucoside, has been 13C-labelled at C-2 of the flavonoid unit by synthesis in 15% yield over five steps from [13C]carbon dioxide. The route is appropriate for radiochemical synthesis. Formation of the protected 3-glucosylated flavonol appears to result from [1,7]-sigmatropic rearrangement with migration of a benzyl group followed by cyclisation. A free 5-OH results even when a phosphazene superbase is used.