101413-30-3

Basic information

• Product Name: 1-(5'-phenyl-[1,1':3',1''-terphenyl]-2'-yl)ethanone
• Synonyms: 1-(5'-phenyl-[1,1':3',1''-terphenyl]-2'-yl)ethanone
• CAS NO: 101413-30-3
• Molecular Weight: 348.444
• Mol File: 101413-30-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1-(5'-phenyl-[1,1':3',1''-terphenyl]-2'-yl)ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(5'-phenyl-[1,1':3',1''-terphenyl]-2'-yl)ethanone(101413-30-3)
• EPA Substance Registry System: 1-(5'-phenyl-[1,1':3',1''-terphenyl]-2'-yl)ethanone(101413-30-3)

Safety Data

• Hazardous Substances Data: 101413-30-3(Hazardous Substances Data)

Upstream product

• 1504-72-9 ethyl 3-phenylbut-2-enoate 
• 704-79-0 3-phenylbut-2-enoic acid 
• 25354-72-7 2-benzylidene-1-phenyl-butane-1,3-dione 
• 93-91-4 1-phenylbutan-1,3-dione 
• 26456-18-8 5-Dimethylamino-1,3,5-triphenyl-pent-2,4-dien-1-on 
• 67-64-1 acetone 
• 1484-88-4 2,4,6-triphenylpyrilium perchlorate 
• 495-45-4 dypnone 
• 98-86-2 acetophenone 
• 141-52-6 sodium ethanolate 
• 33733-07-2 5'-methyl-1,1':3',1''-terphenyl 
• 98-88-4 benzoyl chloride 

Downstream Products

• 65-85-0 benzoic acid 
• 113710-69-3 2-Benzoyl-3,5-diphenyl-benzoesaeure 

Relevant articles and documents

Construction of Multi-Substituted Benzenes via NHC-Catalyzed Reactions of Carboxylic Esters

A carbene-catalyzed ester activation reaction for the synthesis of multi-substituted benzenes is developed. Tetra-substituted benzene compounds are efficiently synthesized through this methodology. Compared with aldehyde substrates used in previous reports, the ester substrates used here are much more readily available and inexpensive. In addition, the TEMPO oxidant used here is more inexpensive than the quinones commonly used in related carbene-catalyzed reactions.

Pyrylium Compounds. XXIX. Substituted Benzophenones from 2,4,6-Triarylpyrylium Salts and Methyl(ene) Ketones

In the presence of piperidine acetate (or similar salts of certain dialkylamines), 2,4,6-triarylpyrylium perchlorates 5 react with methyl(ene) ketones 6 to give benzophenones 7, the structure of which was proved by spectroscopic methods as well as by independent synthesis.Besides acetone and other acyclic ketones (e. g. alkyl methyl ketones, phenylacetone, desoxybenzoin, dibenzyl ketone) cyclic ketones (e. g. cyclopentanone, cyclohexanone, cycloheptanone, acenaphthenone) can also be used as ketone component 6; acetophenones react differently leading to hydrocarbons of the 1,3,5-triarylbenzene type 15.The varying efficiency of the diverse amine salts and the mode of incorporation of the unsymmetrically substituted ketones suggest the intermediate formation of enamines 10 as crucial step of the ring transformations observed.This assumption is supported by isolation of the iminium salt 18 on reacting 3,5-dimethyl-2,4,6-triphenylpyrylium perchlorate (16) with acetone/piperidine acetate.