72036-41-0

Basic information

• Product Name: 4'-METHYL-2,2':6',2''-TERPYRIDINE
• Synonyms: 4'-METHYL-2,2':6',2''-TERPYRIDINE
• CAS NO: 72036-41-0
• Molecular Formula: C₁₆H₁₃N₃
• Molecular Weight: 247.29
• Mol File: 72036-41-0.mol
• Article Data: 10

Chemical Properties

• Boiling Point: 401.464 °C at 760 mmHg
• Flash Point: 178.511 °C
• Appearance: /
• Density: 1.145 g/cm³
• CAS DataBase Reference: 4'-METHYL-2,2':6',2''-TERPYRIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4'-METHYL-2,2':6',2''-TERPYRIDINE(72036-41-0)
• EPA Substance Registry System: 4'-METHYL-2,2':6',2''-TERPYRIDINE(72036-41-0)

Safety Data

• Hazardous Substances Data: 72036-41-0(Hazardous Substances Data)

Usage

General Description

4'-Methyl-2,2':6',2''-terpyridine is a chemical compound with a molecular formula C 21 H 15 N 3. It is a member of the terpyridine family, which is known for its versatile coordination chemistry and application in materials science. 4'-Methyl-2,2':6',2''-terpyridine has been studied for its potential use in optical and electronic devices, such as light-emitting diodes and photovoltaic cells. It has also been investigated for its coordination with metal ions, making it a potential building block for coordination polymers and metal-organic frameworks. Additionally, this compound has been explored as a fluorescent probe for detecting metal ions in biological and environmental samples. Overall, 4'-methyl-2,2':6',2''-terpyridine shows promise for various applications in chemistry and materials science due to its unique structure and versatile coordination behavior.

Upstream product

• 119715-60-5 (E)-1-(pyridine-2-yl)-N-(pyridine-2-ylmethylene)methaneamine 
• 81874-50-2 3-(methylsulfanyl)-1,5-di(pyridin-2-yl)pent-2-ene-1,5-dione 
• 78570-34-0 3,3-bis(methylsulfanyl)-1-pyridin-2-ylprop-2-en-1-one 
• 1122-62-9 2-acetylpyridine 
• 626-51-7 3-methyl glutaric acid 
• 19013-37-7 dimethyl 3-methylglutarate 
• 4664-16-8 4-methyl-2,6-dihydroxypyridine 
• 73112-16-0 2,6-Dibromo-4-methylpyridine 
• 17997-47-6 2-tri-n-butylstannylpyridine 
• 207804-48-6 3-Methyl-1,5-di-pyridin-2-yl-pentane-1,5-dione 
• 594-27-4 tetramethylstannane 
• 134653-69-3 4'-{[(Trifluoromethyl)sulfonyl]oxy}-2,2':6',2''-terpyridine 
• 75-16-1 methylmagnesium bromide 
• 78570-35-1 2,6-bis(2-pyridinyl)-4-(methylthio)pyridine 

Downstream Products

• 152793-28-7 4'-(2'''-Phenylethyl)-2,2':6',2''-terpyridine 
• 152793-37-8 4'-<2'''-(4''''-Nitrophenyl)ethyl>-2,2':6',2''-terpyridine-6,6''-dicarbonitrile 
• 152793-33-4 4'-<2'''-(4''''-Nitrophenyl)ethyl>-2,2':6',2''-terpyridine N,N''-dioxide 
• 152793-29-8 4'-<2'''-(4''''-Nitrophenyl)ethyl>-2,2':6',2''-terpyridine 
• 208597-43-7 4'-((diphenylphosphinoyl)methylene)-2,2':6',2''-terpyridine 
• 536696-95-4 4'-[bis-(diphenyl-phosphinoyl)-methyl]-[2,2';6',2'']terpyridine 
• 288103-61-7 4'-[bis(diphenylphosphino)methane]-2,2':6',2''-terpyridine 
• 288103-62-8 4'-[(Diphenylphosphanyl)-methyl]-[2,2';6',2'']terpyridine 
• 167026-72-4 4'-Hentriacontyl-2,2':6',2''-terpyridine 
• 108295-45-0 4′-formyl-2,2′:6′2″-terpyridine 

Relevant articles and documents

Compound for molecular electronic device having thiol anchoring group, method of synthesizing the compound, and molecular electronic device having molecular active layer obtained from the compound

Provided are a compound for a molecular electronic device which includes a terpyridine-ruthenium organic metal compound including a thiol anchoring group of the formula below, a method of synthesizing the compound and a molecular electronic device including a molecular active layer obtained from the compound. In the formula, R1 and R2 are each a thioacetyl group or a hydrogen atom, at least one of R1 and R2 is a thioacetyl group, and m and n are each integers from 0 to 20. The molecular active layer, which is formed by self-assembling the compound on an electrode surface, composes a switching element and a memory element.

Bucky ligands: Synthesis, Ruthenium(II) complexes, and electrochemical properties

The novel tridentate 2,2':6',2-terpyridine ligand (1) in which the metal-binding domain is directly attached to a methanofullerene C60 unit was incorporated into ruthenium-based diads and triads that may undergo photoinduced charge s

Photoinduced electron- and energy-transfer processes occurring within porphyrin-metal-bisterpyridyl conjugates

Photophysical properties have been measured for zinc and free-base porphyrins covalently linked to ruthenium-(II) or rhodium(III) bisterpyridyl complexes using ultrafast transient absorption spectroscopy. The appended metal complex quenches porphyrin fluo