483370
2,6-双(2-吡啶基)-4(1H)-吡啶酮
98%
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关于此项目
经验公式（希尔记法）:
C15H11N3O
化学文摘社编号:
分子量:
249.27
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
产品名称
2,6-双(2-吡啶基)-4(1H)-吡啶酮, 98%
InChI
1S/C15H11N3O/c19-11-9-14(12-5-1-3-7-16-12)18-15(10-11)13-6-2-4-8-17-13/h1-10H,(H,18,19)
SMILES string
O=C1C=C(NC(=C1)c2ccccn2)c3ccccn3
InChI key
HRORSVNZQWCZTD-UHFFFAOYSA-N
assay
98%
mp
168-170 °C (lit.)
Quality Level
Application
2,6-Bis(2-pyridyl)-4(1H)-pyridone can be used a heterocyclic building block to prepare 4′-substituted terpyridines by reacting with ω-substituted primary alcohols or nucleosides via Mitsunobu reaction. It is also used to prepare cyclotriphosphazene ligands with pendant terpyridine moieties.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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
Toward an iron (II) spin-crossover grafted phosphazene polymer
Davidson RJ, et al.
Inorganic Chemistry, 51(15), 8307-8316 (2012)
Synthesis of 4?-substituted 2, 2?: 6?, 2 ?-terpyridines via a Mitsunobu reaction
Hovinen J
Tetrahedron Letters, 45(29), 5707-5709 (2004)
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