13249-75-7

Usage

Appearance

Yellow crystalline powder

Usage

a. Organic synthesis
b. Chemical intermediate
c. Building block in pharmaceuticals and agrochemicals

Potential properties

a. Anti-inflammatory
b. Anti-cancer
c. Anti-microbial

Applications in medicinal chemistry

Valuable and versatile chemical

Investigated for

a. Materials science
b. Development of organic electronic devices
c. Development of sensors

InChI:InChI=1/C22H16O2/c23-21(18-12-6-2-7-13-18)16-20(17-10-4-1-5-11-17)22(24)19-14-8-3-9-15-19/h1-16H

Upstream product

• 67-66-3 chloroform 
• 6307-20-6 2,3,5-triphenylfuran 
• 546-67-8 lead(IV) tetraacetate 
• 64-19-7 acetic acid 
• 13901-77-4 1-methyl-2,3,5-triphenyl-1H-pyrrole 
• 64-17-5 ethanol 
• 141-52-6 sodium ethanolate 
• 98-86-2 acetophenone 
• 134-81-6 benzil 
• 60-29-7 diethyl ether 
• 959-28-4 1,4-diphenylbut-2-ene-1,4-dione 
• 20913-05-7 (Benzoylmethylene)triphenylphosphorane 
• 112484-32-9 2-(2,3,5-triphenyl-pyrrol-1-yl)-ethanol 
• 7722-84-1 dihydrogen peroxide 

Downstream Products

• 102662-06-6 3-chloro-2,4,5-triphenyl-furan 
• 4441-01-4 1,2,4-triphenylbutane-1,4-dione 
• 6307-20-6 2,3,5-triphenylfuran 
• 20851-07-4 2,3,5-triphenylthiophene 
• 857821-60-4 3-bromo-2,5-bis-(4-bromo-phenyl)-4-phenyl-furan 
• 28665-87-4 2-morpholin-4-yl-1,3,4-triphenyl-butane-1,4-dione 
• 76-93-7 Benzilic acid 
• 134-81-6 benzil 
• 51265-75-9 3,5,6-triphenyl-6H-1,2-oxazin-6-ol 
• 2272-58-4 3,4,6-triphenyl-pyridazine 
• 56625-34-4 acetic acid-(triphenyl-[3]furyl ester) 
• 65-85-0 benzoic acid 
• 36372-77-7 1,4,5-triphenyl-1H-pyrazole 
• 3274-61-1 2,4,5-triphenylpyrrole 

Relevant academic research and scientific papers

Simple, efficient, and stereoselective oxidation of triphenylfurans to cis-but-2-ene-1,4-diones

Triphenylfurans are stereoselctively oxidized to cis-but-2-ene-1,4-diones, suitable precursors of 3(2H)-furanones, in very good yields using ammonium nitrate or potassium nitrate in 80% aqueous acetic acid. Copyright Taylor & Francis Group, LLC.

Sequential electrochemical oxidation of alternating benzene-furan oligomers

(Graph Presented) Electrochemical oxidation of pentaaryl 2 containing two furan moieties occurs sequentially to give diketone 8 after two-electron transfer. Further oxidation with another two-electron transfer gives the corresponding tetraketone 9. Radica

A novel one-pot synthesis of substituted pyridazines: A general method of preparation of 3,4,6-tri aryl pyridazines

3,4,6-triaryl pyridazines 4 were conveniently prepared in one step by the condensation of aryl methyl ketones and 1,2-diketones in presence of base, followed by cyclisation with hydrazines.

Oxidation of furans with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ)

2,5-Disubstituted furans were oxidatively cleaved to 2-butene-1,4- diones with DDQ in CH2Cl2-DMSO. In particular, 3-alkoxy-2,5-diphenylfurans were selectively converted into cis-2-alkoxy-1,4-diphenyl-2-butene-1,4-diones with DDQ in C

OXIDATIVE AND BASIC TRANSFORMATIONS OF SOME 1-HETEROARYLOLIGOPHENYLPYRIDINIUM SALTS. LIMITATIONS TO THE APPLICABILITY OF FERRICYANIDE OXIDATION

Ferricyanide oxidation of 2,3,4,6-tetraphenyl-1-(2'-pyridyl)pyridinium perchlorate (III) gave, in addition to the biheterocyclic product Ib,two pyrrole derivatives IIb and IIc and in some conditions also the diketone IV.Additional pyrrole derivatives, VII