1415387-42-6

Basic information

• Product Name: 4-(1-(5-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethyllbenzoyl)piperidin-4-yl)benzonitrile
• Synonyms: 4-(1-(5-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethyllbenzoyl)piperidin-4-yl)benzonitrile
• CAS NO: 1415387-42-6
• Molecular Weight: 514.424
• Mol File: 1415387-42-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 4-(1-(5-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethyllbenzoyl)piperidin-4-yl)benzonitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-(5-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethyllbenzoyl)piperidin-4-yl)benzonitrile(1415387-42-6)
• EPA Substance Registry System: 4-(1-(5-(6-bromo-3H-imidazo[4,5-b]pyridin-2-yl)-2,4-dimethyllbenzoyl)piperidin-4-yl)benzonitrile(1415387-42-6)

Safety Data

• Hazardous Substances Data: 1415387-42-6(Hazardous Substances Data)

Upstream product

• 611-01-8 2,4-dimethyl-benzoic acid 
• 162997-34-4 4-(piperidin-4-yl)benzonitrile hydrochloride 
• 162997-33-3 tert-butyl 4-(4-cyanophenyl)piperidine-1-carboxylate 
• 460365-08-6 4-(4-cyanophenyl)-3,6-dihydro-2H-pyridine-1-carboxylic acid tert-butyl ester 
• 871112-38-8 tert-butyl 4-(4-cyanophenyl)-4-hydroxypiperidine-1-carboxylate 
• 163209-96-9 tert-butyl 4-(4-bromophenyl)-4-hydroxypiperidine-1-carboxylate 
• 79099-07-3 N-tert-butyloxycarbonylpiperidin-4-one 
• 589-87-7 1,4-bromoiodobenzene 
• 38875-53-5 5-bromo-pyridine-2,3-diamine 
• 1399181-27-1 4-(1-(5-formyl-2,4-dimethylbenzoyl)piperidin-4-yl)benzonitrile 
• 742081-03-4 5-iodo-2,4-dimethylbenzoic acid 

Relevant articles and documents

TCNE-decorated triphenylamine-based conjugated polymer: Click synthesis and efficient turn-on fluorescent probing for Hg2+

A type of triphenylamine-based conjugated polymer with cyano-containing chromophore in side chain, poly[(9,9-dioctyl)-2,7-fluorene-co-N-4-(1,1,4,4- tetracyanobuta-1,3-dienyl)-4,4′-triphenylamine] (P3) was successfully synthesized by catalyst-free and efficient click reaction between poly[(9,9-dioctyl)-2,7-fluorene-co-N-4-ethynyl-4,4′-triphenylamine] (P2) and tetracyanoethylene (TCNE). Chemical structures of intermediates and target polymer were verified by FT-IR and 1H NMR analyses. Fluorescence of P3's THF solution was specifically quenched by the introduction of I -, accompanied by the change of its apparent color from pale brown to light yellow. With the introduction of Hg2+, fluorescence of P3/I- complex recovered quickly and even exceeded the initial intensity of pristine P3 (when the concentration of Hg2+ above ～6.65 × 10-5 M). Other common cations brought very slight interference for P3/I- complex's response of Hg2+, and the detection limit of Hg2+ reached ～6.9 nM for such probing system.2013 Elsevier Ltd. All rights reserved.