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(Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide

Base Information Edit
  • Chemical Name:(Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide
  • CAS No.:1447693-81-3
  • Molecular Formula:C28H35N5O
  • Molecular Weight:457.619
  • Hs Code.:
  • Mol file:1447693-81-3.mol
(Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide

Synonyms:(Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide

Suppliers and Price of (Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of (Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide Edit
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Technology Process of (Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide

There total 3 articles about (Z)-7-(2,3-di-p-tolyl-7,8-dihydropyrido[2,3-b]pyrazin-5(6H)-yl)-N'-hydroxyheptanimidamide 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 hydroxylamine hydrochloride; potassium carbonate; In ethanol; for 72h; Inert atmosphere; Reflux;
Guidance literature:
Multi-step reaction with 2 steps
1: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C
2: potassium carbonate; hydroxylamine hydrochloride / ethanol / 72 h / Inert atmosphere; Reflux
With hydroxylamine hydrochloride; sodium tris(acetoxy)borohydride; potassium carbonate; In ethanol; 1,2-dichloro-ethane;
Guidance literature:
Multi-step reaction with 3 steps
1: trimethylamine-N-oxide / dimethyl sulfoxide / 20 °C / Inert atmosphere
2: sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 20 °C
3: potassium carbonate; hydroxylamine hydrochloride / ethanol / 72 h / Inert atmosphere; Reflux
With trimethylamine-N-oxide; hydroxylamine hydrochloride; sodium tris(acetoxy)borohydride; potassium carbonate; In ethanol; dimethyl sulfoxide; 1,2-dichloro-ethane;
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