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Structure, properties, spectra, suppliers and links for: 3,6-DI-2-PYRIDYL-1,2,4,5-TETRAZINE, 1671-87-0.
3,6-Di(2-pyridinyl)-1,2-dihydro-1,2,4,5-tetraazine | C12H10N6 | CID 286497 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more.
3,6-Di-2-pyridyl-1,2,4,5-tetrazine (DPTZ) undergoes solvothermal reaction with CuSO 4.6H 2 O and Cu(Ac) 2.H 2 O to afford copper containing coordination polymers. It reacts with enamine derivative of morpholine and 5-,6-,7- and 8-membered cyclic ketones to afford pyridazine derivatives.
Lloyd-Jones details how 2-pyridyl boronic acids decompose via fragmentation of a zwitterionic intermediate, which is formed at a maximum rate between pH 4 and 8 (Scheme 11 ). This species is more readily formed from 2-pyridyl boronic acids than the 3- or 4-pyridyl analogues.
Solutions video library VWR product demonstrations and samples ... 3,6-Di(2-pyridyl)-1,2,4,5-tetrazine 96%. 3,6-Di(2-pyridyl)-1,2,4,5-tetrazine ... 11. Engage in any other conduct that restricts or inhibits anyone’s use of the Web Site, or which, as determined by the Company, may harm the Company or users of the Web Site or expose them to ...
Description. 3,6-Di-2-pyridyl-1,2,4,5-tetrazine may be used in the preparation of mononuclear, cyclic tetranuclear, and 1-D helical-chain Cu (II) complexes, via metal-assisted hydrolysis. It also may be used in the synthesis of novel cyclic tetranuclear ZnII complex and synthesis of substituted 3,6-di (2-pyridyl)pyridazines, via inverse ...
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