Tris[4-(1,1-dimethylethyl)-2-(1H-pyrazol-1-yl)pyridine]cobalt salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:3)

Base Information

Chemical Name:Tris[4-(1,1-dimethylethyl)-2-(1H-pyrazol-1-yl)pyridine]cobalt salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:3)
CAS No.:1447938-61-5
Molecular Formula:3C₂F₆NO₄S₂*C₃₆H₄₅CoN₉
Molecular Weight:1503.25
Hs Code.:2933399990

Tris[4-(1,1-dimethylethyl)-2-(1H-pyrazol-1-yl)pyridine]cobalt salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:3)

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Chemical Property of Tris[4-(1,1-dimethylethyl)-2-(1H-pyrazol-1-yl)pyridine]cobalt salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:3)

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Purity/Quality:: 99% ^*data from raw suppliers

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Technology Process of Tris[4-(1,1-dimethylethyl)-2-(1H-pyrazol-1-yl)pyridine]cobalt salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:3)

There total 1 articles about Tris[4-(1,1-dimethylethyl)-2-(1H-pyrazol-1-yl)pyridine]cobalt salt with 1,1,1-trifluoro-N-[(trifluoromethyl)sulfonyl]methanesulfonamide (1:3) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: cobalt(II) chloride hexahydrate

: 1361941-59-4
2-(1H-pyrazol-1-yl)-4-tert-butylpyridine

: 90076-65-6
bis(trifluoromethane)sulfonimide lithium

: 1447938-61-5
tris(2-(1H-pyrazol-1-yl)-4-tert-butylpyridine)cobalt(III) tris(bis(trifluoromethylsulfonyl)imide)

Guidance literature:: cobalt(II) chloride hexahydrate; 2-(1H-pyrazol-1-yl)-4-tert-butylpyridine; In methanol; water; at 70 ℃; for 0.166667h;

With hydrogenchloride; dihydrogen peroxide; In methanol; water; at 70 ℃; for 2h;

bis(trifluoromethane)sulfonimide lithium; at 50 ℃;
DOI:10.1021/cm400796u