267668-44-0

Basic information

• Product Name: Methanone, 1,3,5-benzenetriyltris[(4-fluorophenyl)-
• CAS NO: 267668-44-0
• Molecular Formula: C27H15F3O3
• Molecular Weight: 444.41
• Mol File: 267668-44-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Methanone, 1,3,5-benzenetriyltris[(4-fluorophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, 1,3,5-benzenetriyltris[(4-fluorophenyl)-(267668-44-0)
• EPA Substance Registry System: Methanone, 1,3,5-benzenetriyltris[(4-fluorophenyl)-(267668-44-0)

Safety Data

• Hazardous Substances Data: 267668-44-0(Hazardous Substances Data)

Upstream product

• 54012-23-6 1-(4-fluorophenyl)prop-2-yn-1-one 
• 462-06-6 fluorobenzene 
• 4422-95-1 1,3,5-benzene tris(carbonyl chloride) 
• 161891-29-8 (Z)-3-chloro-3-(4-fluorophenyl)acrylaldehyde 

Downstream Products

• 416838-88-5 [3,5-bis-(4-hydroxy-benzoyl)-phenyl]-(4-hydroxy-phenyl)-methanone 

Relevant articles and documents

An indole-derived porous organic polymer for the efficient visual colorimetric capture of iodine in aqueous media: Via the synergistic effects of cation-π and electrostatic forces

We have successfully synthesized a novel type of recyclable indole-based porous polymer, which possesses highly effective capture behavior for iodine in aqueous solution via the synergistic effects of cation-π and electrostatic forces. More interestingly,

A Method for Preparation of [3,5-bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone

The present invention relates to a method for preparing a cyclic olefin polymer [3,5-bis(4-fluorobenzoyl)phenyl](4-fluorophenyl)methanone. More specifically, the present invention improves the reaction time and the amount of the raw material and non-solve

Convenient access to 1,3,5-triaroylbenzenes

The unusual transformation of β-aryl-β-haloacroleins into valuable triaroylbenzenes is reported by the first time. The convenient sequence takes advantage on the one step access to triaroylbenzenes. This work establishes that the presence of amine is required for the trimerization procedure since it is involved in the formation of iminium-enamine intermediate A.