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4-benzylidene-3-(4-methoxy-phenyl)-4H-isoxazol-5-one

Base Information Edit
  • Chemical Name:4-benzylidene-3-(4-methoxy-phenyl)-4H-isoxazol-5-one
  • CAS No.:35113-43-0
  • Molecular Formula:C17H13NO3
  • Molecular Weight:279.295
  • Hs Code.:
  • Mol file:35113-43-0.mol
4-benzylidene-3-(4-methoxy-phenyl)-4<i>H</i>-isoxazol-5-one

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 4-benzylidene-3-(4-methoxy-phenyl)-4H-isoxazol-5-one Edit
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Technology Process of 4-benzylidene-3-(4-methoxy-phenyl)-4H-isoxazol-5-one

There total 4 articles about 4-benzylidene-3-(4-methoxy-phenyl)-4H-isoxazol-5-one 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 piperidine; In isopropyl alcohol; at 50 ℃; for 2h; Inert atmosphere;
DOI:10.1002/anie.201410933
Guidance literature:
Multi-step reaction with 3 steps
1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 80 °C / Inert atmosphere; Reflux
2: hydroxylamine hydrochloride; potassium carbonate / ethanol; water / 20 h / 22 °C / Inert atmosphere
3: piperidine / isopropyl alcohol / 2 h / 50 °C / Inert atmosphere
With piperidine; hydroxylamine hydrochloride; sodium hydride; potassium carbonate; In tetrahydrofuran; ethanol; water; isopropyl alcohol; mineral oil;
DOI:10.1002/anie.201410933
Guidance literature:
Multi-step reaction with 2 steps
1: hydroxylamine hydrochloride; potassium carbonate / ethanol; water / 20 h / 22 °C / Inert atmosphere
2: piperidine / isopropyl alcohol / 2 h / 50 °C / Inert atmosphere
With piperidine; hydroxylamine hydrochloride; potassium carbonate; In ethanol; water; isopropyl alcohol;
DOI:10.1002/anie.201410933
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