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2,2':6',2''-Terpyridine

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2,2':6',2''-Terpyridine Basic information
Application in coordination chemistry
Product Name:2,2':6',2''-Terpyridine
Synonyms:2,2':6',2''-Terpyridine,97%;2,2′:6′,2′′-Terpyridine ,98%;6',2'']Terpyridine;2,2',2" TERPYRIDINE (Tripyridine, Tripyridyl);´;2,2':6',2"-Terpyridine 98%;2,6-BIS(PYRIDIN-2-YL)PYRIDINE;TIMTEC-BB SBB008932
CAS:1148-79-4
MF:C15H11N3
MW:233.27
EINECS:214-559-5
Product Categories:Pyrimidines;Achiral Nitrogen;Py-N
Mol File:1148-79-4.mol
2,2':6',2''-Terpyridine Structure
2,2':6',2''-Terpyridine Chemical Properties
Melting point 90-93 °C
Boiling point 370 °C
density 1.1901 (rough estimate)
refractive index 1.5610 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility dioxane: 0.1 g/mL, clear
form Crystalline powder
pka4.60±0.10(Predicted)
color Cream to yellow to brown
Water Solubility 1.472g/L(24.99 ºC)
BRN 11199
InChIInChI=1S/C15H11N3/c1-3-10-16-12(6-1)14-8-5-9-15(18-14)13-7-2-4-11-17-13/h1-11H
InChIKeyDRGAZIDRYFYHIJ-UHFFFAOYSA-N
SMILESC1(C2=NC(C3=NC=CC=C3)=CC=C2)=NC=CC=C1
CAS DataBase Reference1148-79-4(CAS DataBase Reference)
EPA Substance Registry System2,2':6',2''-Terpyridine (1148-79-4)
Safety Information
Hazard Codes T+,T
Risk Statements 27/28-37/38-41
Safety Statements 26-28-36/37/39-45
RIDADR UN 2811 6.1/PG 1
WGK Germany 3
TSCA TSCA listed
HazardClass 6.1
PackingGroup I
HS Code 29333990
Storage Class6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials
Hazard ClassificationsAcute Tox. 1 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2,2':6',2''-Terpyridine Usage And Synthesis
Application in coordination chemistry

As an NNN-tridentate ligand, the 2,2′:6′,2″-terpyridine plays an important role in coordination chemistry. With three coordination sites and low LUMO, terpyridine and its derivatives are one of the typical Pincer ligand and/or non-innocent ligands in transition metal catalysis. Interesting catalytic reactivities have been obtained with these tpy-metal complexes targeting some challenging transformations, such as C–C bond formation and hydrofunctionalization. The 2,2':6':2''-terpyridine ligand has literally shaped the coordination chemistry of transition metal complexes in a plethora of fields.

Description2,2':6',2''-Terpyridine is a case of occupational dermatitis was reported in a chemical technician, with no cross reactivity to pyridine derivatives.
Chemical PropertiesOff-white crystal
Uses2,2';6',2"-terpyridine is widely utilized in the field of supramolecular chemistry, which is used to manufacture the racks, ladders and grids, helicates, catenanes and dendrimers. It plays an important role as a ligand in coordination chemistry. Its complexes are employed in the oxidation of alcohols, the carbonylation of aromatic compounds and as oxygen-binding molecules. Functionalized terpyridine ligands were used in semiconductors and solar panels. It forms chealate complexes with europium(III) and terbium(III), which is used in protein labelling.
DefinitionChEBI: A tridentate heterocyclic ligand that binds metals at three meridional sites giving two adjacent 5-membered MN2C2 chelate rings.
Synthesis Reference(s)Journal of the American Chemical Society, 103, p. 3585, 1981 DOI: 10.1021/ja00402a062
Organic Syntheses, Coll. Vol. 7, p. 476, 1990
General Description2,2′:6′,2′′;-Terpyridine is a tridentate ligand that can be prepared in two steps starting from 2-acetylpyridine.
Contact allergensThis molecule is a terpyridine with a 4-methyl substitution. A case of occupational dermatitis was reported in a chemical technician with no cross-reactivity to pyridine derivatives.
Purification MethodsCrystallise it from diethyl ether, toluene or from pet ether, then aqueous MeOH, followed by sublimation in a vacuum at 90o. It is used for estimating Ag and Ru. [Kamra et al. Anal Chim Acta 81 177 1976, Beilstein 26 III/IV 258.]
Tag:2,2':6',2''-Terpyridine(1148-79-4) Related Product Information
6''-Chloro-[3,2':5',3'']-terpyridine 2,2':6',2''-Terpyridine 1,6-DIHYDRO-[3,2':4',3'']-TERPYRIDINE [2,2':6',2''-Terpyridine]-3',4'-dicarboxylic acid 4'-Chloro-2,2':6',2''-terpyridine 4,4',4''-Tri-tert-butyl-2,2':6',2''-terpyridine 5-Methyl-4'-nitro-2,2':6',2''-terpyridine 4'-(4-Nitrophenyl)-2,2':6',2''-terpyridine 2,2':6',2''-Terpyridine-4'-carboxylic acid 4'-Iodo-2,2':6',2''-terpyridine 6,6''-Dimethyl-[2,2':6',2''-terpyridine]-4'-carboxylic acid ethyl ester 4'-Phenyl-2,2':6',2''-terpyridine 4',4''''-(1,4-Phenylene)bis(2,2':6',2''-terpyridine) Ethyl 2,2':6',2''-terpyridine-4'-carboxylate 5,5''-Dimethyl-[2,2':6',2''-terpyridine]-4'-carboxylic acid 5,5''-Dimethyl-[2,2':6',2''-terpyridine]-4'-carboxylic acid ethyl ester [2,2':6',2''-Terpyridine]-4'-carboxylic acid butyl ester Dichloro(2 2':6' 2''-terpyridine)-