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C41H36N6O2

Base Information
  • Chemical Name:C41H36N6O2
  • CAS No.:1400934-09-9
  • Molecular Formula:C41H36N6O2
  • Molecular Weight:644.776
  • Hs Code.:
C<sub>41</sub>H<sub>36</sub>N<sub>6</sub>O<sub>2</sub>

Synonyms:

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Chemical Property of C41H36N6O2
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Technology Process of C41H36N6O2

There total 16 articles about C41H36N6O2 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:
With sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene; In water; tert-butyl alcohol; at 20 ℃; for 1h;
DOI:10.1016/j.ejmech.2012.07.040
Guidance literature:
Multi-step reaction with 10 steps
1.1: n-butyllithium; 2,2,6,6-tetramethylpiperidinyl-lithium / tetrahydrofuran; hexane / 0.08 h / -78 - -10 °C / Inert atmosphere
1.2: 5 h / -78 - 20 °C / Inert atmosphere
2.1: toluene / 20 °C
3.1: tetrakis(triphenylphosphine) palladium(0); potassium carbonate / ethanol; toluene / 4 h / 100 °C / Inert atmosphere
4.1: trimethylsilylazide; trifluoroacetic acid / 36 h / 120 °C / Sealed tube
5.1: triethylamine / dichloromethane / 1 h / 20 °C
6.1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 8 h / Reflux
7.1: acetonitrile / 12 h / 70 °C
8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 8 h / Inert atmosphere; Reflux
9.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / -78 °C
9.2: 1 h / -60 - 20 °C
10.1: sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene / water; tert-butyl alcohol / 1 h / 20 °C
With sodium chlorite; sodium dihydrogenphosphate; N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; 2-methyl-but-2-ene; oxalyl dichloride; trimethylsilylazide; 2,2,6,6-tetramethylpiperidinyl-lithium; tetrabutyl ammonium fluoride; potassium carbonate; triethylamine; trifluoroacetic acid; dibenzoyl peroxide; In tetrahydrofuran; tetrachloromethane; ethanol; hexane; dichloromethane; water; dimethyl sulfoxide; toluene; acetonitrile; tert-butyl alcohol; 3.1: |Suzuki Coupling / 9.1: |Swern Oxidation / 9.2: |Swern Oxidation;
DOI:10.1016/j.ejmech.2012.07.040
Guidance literature:
Multi-step reaction with 5 steps
1: trimethylsilylazide; trifluoroacetic acid / 36 h / 120 °C / Sealed tube
2: triethylamine / dichloromethane / 1 h / 20 °C
3: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 8 h / Reflux
4: potassium carbonate / N,N-dimethyl-formamide / 18 h / 20 °C / Inert atmosphere
5: sodium chlorite; sodium dihydrogenphosphate; 2-methyl-but-2-ene / water; tert-butyl alcohol / 1 h / 20 °C
With sodium chlorite; sodium dihydrogenphosphate; N-Bromosuccinimide; 2-methyl-but-2-ene; trimethylsilylazide; potassium carbonate; triethylamine; trifluoroacetic acid; dibenzoyl peroxide; In tetrachloromethane; dichloromethane; water; N,N-dimethyl-formamide; tert-butyl alcohol;
DOI:10.1016/j.ejmech.2012.07.040
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