33733-07-2

Basic information

• Product Name: 1,1':3',1''-Terphenyl, 5'-methyl-
• CAS NO: 33733-07-2
• Molecular Formula: C19H16
• Molecular Weight: 244.336
• Mol File: 33733-07-2.mol

Chemical Properties

• CAS DataBase Reference: 1,1':3',1''-Terphenyl, 5'-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1':3',1''-Terphenyl, 5'-methyl-(33733-07-2)
• EPA Substance Registry System: 1,1':3',1''-Terphenyl, 5'-methyl-(33733-07-2)

Safety Data

• Hazardous Substances Data: 33733-07-2(Hazardous Substances Data)

Usage

Type of compound

Chemical compound

Structure

A derivative of terphenyl, a hydrocarbon consisting of three connected benzene rings

Functional groups

Methyl group at the 5' position

Applications

a. Building block in the synthesis of various organic compounds
b. Production of dyes
c. Production of polymers
d. Production of pharmaceuticals

Fluorescent properties

Useful in the development of fluorescent probes and sensors for scientific research and medical diagnostics

Electronic and optical properties

Studied for potential use in organic electronic devices

Upstream product

• 1484-88-4 2,4,6-triphenylpyrilium perchlorate 
• 67-64-1 acetone 

Downstream Products

• 101413-30-3 1-(5'-phenyl-[1,1':3',1''-terphenyl]-2'-yl)ethanone 
• 65-85-0 benzoic acid 
• 62-23-7 4-nitro-benzoic acid 
• 741671-58-9 [3,5-bis-([1,1';3',1'']terphenyl-5'-ylmethoxy)-phenyl]-methanol 
• 741671-59-0 C₄₅H₃₅BrO₂ 
• 741671-56-7 3,5-bis-([1,1';3',1'']terphenyl-5'-ylmethoxy)-benzoic acid methyl ester 
• 554-95-0 benzene-1,3,5-tricarboxylic acid 
• 113710-69-3 2-Benzoyl-3,5-diphenyl-benzoesaeure 
• 1255762-79-8 1-[1,1';3',1'']terphenyl-5'-ylmethyl-1H-benzoimidazole 
• 297154-61-1 2,5-bis(3,5-diphenylphenyl)-3-phenyl-4-(3-biphenyl)cyclopentadienone 
• 297154-58-6 2,5-bis(3,5-diphenylphenyl)-3,4-diphenylcyclopentadienone 
• 297154-57-5 1,3-bis(3,5-diphenylphenyl)acetone 

Relevant articles and documents

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.