496375
4′-(4-甲基苯基)-2,2′:6′,2′′-三吡啶
98%
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关于此项目
经验公式（希尔记法）:
C22H17N3
化学文摘社编号:
分子量:
323.39
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
产品名称
4′-(4-甲基苯基)-2,2′:6′,2′′-三吡啶, 98%
assay
98%
InChI
1S/C22H17N3/c1-16-8-10-17(11-9-16)18-14-21(19-6-2-4-12-23-19)25-22(15-18)20-7-3-5-13-24-20/h2-15H,1H3
SMILES string
Cc1ccc(cc1)-c2cc(nc(c2)-c3ccccn3)-c4ccccn4
InChI key
IDJYBUVHZHLIIT-UHFFFAOYSA-N
mp
167-170 °C (lit.)
Quality Level
Application
4′-(4-Methylphenyl)-2,2′:6′,2′′-terpyridine may be used as a ligand in the synthesis of:
- terpyridine Ru(II) complexes
- terpyridine based Cd(II) and Hg(II) complexes
- heterobimetallic Ru(II)-Os(II) complexes
General description
4′-(4-Methylphenyl)-2,2′:6′,2′′-terpyridine is a tridentate oligopyridine ligand. Its crystalline structure has been investigated.
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Photoinduced intramolecular energy transfer and anion sensing studies of isomeric RuII OsII complexes derived from an asymmetric phenanthroline-terpyridine bridge.
Maity D, et al.
Dalton Transactions, 43(4), 1829-1845 (2014)
K Yamamoto et al.
Life sciences, 59(25-26), 2139-2146 (1996-01-01)
We have identified 4'-(4-methylphenyl)-2,2':6',2-terpyridine: trihydrochloride (SS701), which belongs to a family of a small unique neuroprotective agents. SS701 accelerated the production of nerve growth factor (NGF) in cultured astroglial cells, dose- and time-dependently. In in vivo studies, SS701, when administered
4'-(4-Methylphenyl)-2,2':6',2''-terpyridine.
Liu HG, et al.
Acta Crystallographica Section E, Structure Reports Online, 63(12), o4876-o4876 (2007)
Synthesis, characterization and electrochemistry of 4'-functionalized 2,2':6',2?-terpyridine ruthenium(II) complexes and their biological activity.
Anthonysamy A, et al.
Dalton Transactions, 16, 2136-2143 (2008)
Synthesis, crystal structure and thermal properties of Cd(II) and Hg(II) terpyridine based compounds.
Saghatforoush L, et al.
Main Group Chemistry, 13(1), 29-39 (2014)
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