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N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine

Base Information
  • Chemical Name:N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine
  • CAS No.:1224881-08-6
  • Molecular Formula:C24H38N6
  • Molecular Weight:410.606
  • Hs Code.:
N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine

Synonyms:N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine

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Chemical Property of N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine
Chemical Property:
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Technology Process of N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine

There total 1 articles about N,N’-dicyclohexyl-2,2-bis-(3,5-dimethylpyrazol-1-yl)-acetamidine 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:
Guidance literature:
1,1'-methylenebis(3,5-dimethyl-1H-pyrazole); With n-butyllithium; In tetrahydrofuran; hexanes; at -70 - -10 ℃;
dicyclohexyl-carbodiimide; In tetrahydrofuran; hexanes; at -70 - 20 ℃;
DOI:10.1016/j.molcata.2009.10.021
Guidance literature:
In tetrahydrofuran; exclusion of air and moisture; soln. of scorpionate ligand in THF added to suspn. of metal salt in THF at room temp., mixt. allowed to react at room temp. overnight; evapn. under vac., CH2Cl2 added to residue, centrifugation, soln. concd.under vac., pptd. by slow addn. of hexane, solid filtered off, washed w ith hexane, dried under vac.; elem. anal.;
DOI:10.1016/j.molcata.2009.10.021
Guidance literature:
With butyllithium; In tetrahydrofuran; hexane; exclusion of air and moisture; soln. of scorpionate ligand in THF added to soln. of metal triflate in THF at room temp., freshly prepd. soln. ofBuLi in hexane/THF added dropwise after 20 min, mixt. allowed to react at room temp. for 12 h; evapn. (vac.), CH2Cl2 added, centrifugation, soln. concd. (vac.), hexaneslowly added, solid filtered off, dissolved in Et2O/THF (20/1), soln. f iltered, filtrate concd. (vac.), hexane added, solid isolated, washed with hexane, dried (vac.); elem. anal.;
DOI:10.1016/j.molcata.2009.10.021
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