55097-58-0

Basic information

• Product Name: (4-methoxyphenyl)[3-(4-methoxyphenyl)oxiran-2-yl]methanone
• Synonyms: Methanone, (4-methoxyphenyl)[3-(4-methoxyphenyl)-2-oxiranyl]-
• CAS NO: 55097-58-0
• Molecular Formula: C₁₇H₁₆O₄
• Molecular Weight: 284.3065
• Mol File: 55097-58-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 464.8°C at 760 mmHg
• Flash Point: 207.5°C
• Density: 1.217g/cm³
• Vapor Pressure: 8.09E-09mmHg at 25°C
• Refractive Index: 1.585
• CAS DataBase Reference: (4-methoxyphenyl)[3-(4-methoxyphenyl)oxiran-2-yl]methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-methoxyphenyl)[3-(4-methoxyphenyl)oxiran-2-yl]methanone(55097-58-0)
• EPA Substance Registry System: (4-methoxyphenyl)[3-(4-methoxyphenyl)oxiran-2-yl]methanone(55097-58-0)

Safety Data

• Hazardous Substances Data: 55097-58-0(Hazardous Substances Data)

Upstream product

• 123-11-5 4-methoxy-benzaldehyde 
• 2196-99-8 2-chloro-1-(4-methoxyphenyl)ethanone 
• 2373-89-9 4,4'-dimethoxychalcone 
• 41564-67-4 (E)-1,3-bis(4-methoxyphenyl)-2-propene-1-one 
• 100-06-1 1-(4-methoxyphenyl)ethanone 

Downstream Products

• 150881-79-1 1,3-bis(4-methoxyphenyl)propane-1,2-dione 
• 170238-95-6 4,5-bis(4-methoxyphenyl)isoxazole 
• 52578-09-3 2,3-bis(4-methoxyphenyl)-3-chloro-2-prop-2-ene aldehyde 
• 120-44-5 1,4-di(4-methoxyphenyl)ethanone 
• 144398-24-3 3,7,8-tris(4-hydroxyphenyl)-1H-pyrrolo[2,1-c][1,4]oxazin-1-one 
• 170238-97-8 1H-3,7,8-tris(4-methoxyphenyl)pyrrolo<2,1-c><1,4>-oxazin-1-one 
• 170238-94-5 3,4-bis(4-methoxyphenyl)-1H-pyrrole-2-carboxylic acid methyl ester 
• 170238-96-7 methyl 3,4-bis(4-methoxyphenyl)-1-[2-(4-methoxyphenyl)-2-oxoethyl]-1H-pyrrole-2-carboxylate 
• 1398119-32-8 (4-methoxyphenyl)(1-(4-methoxyphenyl)naphtho[2,1-b]furan-2-yl)methanone 
• 1226-42-2 1,2-bis(4-methoxyphenyl)-1,2-ethanedione 

Relevant articles and documents

Design, synthesis and cytotoxic activity of certain novel chalcone analogous compounds

A series of chalcone analogous compounds were designed and synthesized. Replacing/substituting the enone or ethylenic bridge of the parent chalcone with rigid heterocyclic moieties or substituted aromatic amines gave nineteen target compounds. Their cytot

Practical approach for preparation of unsymmetric benzils from β-ketoaldehydes

An efficient and practical method for the synthesis of unsymmetric benzils from readily available β-ketoaldehydes has been developed. Various unsymmetric 1,2-diaryldiketones bearing functional groups have been obtained in good to excellent yields under mild reaction conditions. A plausible mechanism was proposed, and α,α-dichloroketone was considered as the key intermediate. The generation of α,α-dichloroketones from β-ketoaldehydes may undergo the following steps: (1) oxidation by sodium hypochlorite, (2) decarboxylation, and (3) chlorination by Cl2 generated from sodium hypochlorite.

A New, Titanium-Mediated Approach to Pyrroles: First Synthesis of Lukianol A and Lamellarin O Dimethyl Ether

-