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N-<2-(4-dimethylaminophenyl)-6-phenylbenzyl>benzimidoyl chloride

Base Information Edit
  • Chemical Name:N-<2-(4-dimethylaminophenyl)-6-phenylbenzyl>benzimidoyl chloride
  • CAS No.:172976-12-4
  • Molecular Formula:C28H25ClN2
  • Molecular Weight:424.973
  • Hs Code.:
  • Mol file:172976-12-4.mol
N-<2-(4-dimethylaminophenyl)-6-phenylbenzyl>benzimidoyl chloride

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-<2-(4-dimethylaminophenyl)-6-phenylbenzyl>benzimidoyl chloride Edit
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Technology Process of N-<2-(4-dimethylaminophenyl)-6-phenylbenzyl>benzimidoyl chloride

There total 8 articles about N-<2-(4-dimethylaminophenyl)-6-phenylbenzyl>benzimidoyl chloride 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:
Multi-step reaction with 9 steps
1: 1.) tetrakis(triphenylphosphine)palladium(0), 2.) sodium carbonate / 1.) 1,2-dimethoxyethane, 20 min, 2.) 1,2-dimethoxyethane, water, reflux
2: 100 percent / hydrogen / Pd/C / ethanol / 1810.02 Torr
4: 99 percent / N-bromosuccinimide, benzoyl peroxide / CCl4 / 2 h / Heating
5: 80 percent / dimethylformamide / Ambient temperature
6: 92 percent / hydrazine hydrate / methanol / 1 h / Heating
7: 73 percent / sodium carbonate / CH2Cl2 / Ambient temperature
8: 1.) tetrakis(triphenylphosphine)palladium(0), 2.) sodium carbonate / 1.) 1,2-dimethoxyethane, 20 min, 2.) 1,2-dimethoxyethane, water, reflux, 45 min
9: chlorodimethylformiminium chloride / SOCl2 / Ambient temperature
With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); Perbenzoic acid; Vilsmeier reagent; hydrogen; sodium carbonate; hydrazine hydrate; palladium on activated charcoal; In methanol; tetrachloromethane; thionyl chloride; ethanol; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 8 steps
1: 100 percent / hydrogen / Pd/C / ethanol / 1810.02 Torr
3: 99 percent / N-bromosuccinimide, benzoyl peroxide / CCl4 / 2 h / Heating
4: 80 percent / dimethylformamide / Ambient temperature
5: 92 percent / hydrazine hydrate / methanol / 1 h / Heating
6: 73 percent / sodium carbonate / CH2Cl2 / Ambient temperature
7: 1.) tetrakis(triphenylphosphine)palladium(0), 2.) sodium carbonate / 1.) 1,2-dimethoxyethane, 20 min, 2.) 1,2-dimethoxyethane, water, reflux, 45 min
8: chlorodimethylformiminium chloride / SOCl2 / Ambient temperature
With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); Perbenzoic acid; Vilsmeier reagent; hydrogen; sodium carbonate; hydrazine hydrate; palladium on activated charcoal; In methanol; tetrachloromethane; thionyl chloride; ethanol; dichloromethane; N,N-dimethyl-formamide;
Guidance literature:
Multi-step reaction with 10 steps
1: 1.) NaNO2, HBr, 2.) CuBr
2: 1.) tetrakis(triphenylphosphine)palladium(0), 2.) sodium carbonate / 1.) 1,2-dimethoxyethane, 20 min, 2.) 1,2-dimethoxyethane, water, reflux
3: 100 percent / hydrogen / Pd/C / ethanol / 1810.02 Torr
5: 99 percent / N-bromosuccinimide, benzoyl peroxide / CCl4 / 2 h / Heating
6: 80 percent / dimethylformamide / Ambient temperature
7: 92 percent / hydrazine hydrate / methanol / 1 h / Heating
8: 73 percent / sodium carbonate / CH2Cl2 / Ambient temperature
9: 1.) tetrakis(triphenylphosphine)palladium(0), 2.) sodium carbonate / 1.) 1,2-dimethoxyethane, 20 min, 2.) 1,2-dimethoxyethane, water, reflux, 45 min
10: chlorodimethylformiminium chloride / SOCl2 / Ambient temperature
With N-Bromosuccinimide; tetrakis(triphenylphosphine) palladium(0); Perbenzoic acid; Vilsmeier reagent; hydrogen bromide; hydrogen; sodium carbonate; hydrazine hydrate; copper(I) bromide; sodium nitrite; palladium on activated charcoal; In methanol; tetrachloromethane; thionyl chloride; ethanol; dichloromethane; N,N-dimethyl-formamide;
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