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Benzamide, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis[N-[(1S)-1-(chloromethyl)-2-phenyleth yl]-

Base Information Edit
  • Chemical Name:Benzamide, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis[N-[(1S)-1-(chloromethyl)-2-phenyleth yl]-
  • CAS No.:630106-27-3
  • Molecular Formula:C34H30Cl2N4O3
  • Molecular Weight:613.543
  • Hs Code.:
  • Mol file:630106-27-3.mol
Benzamide,
3,3'-(1,3,4-oxadiazole-2,5-diyl)bis[N-[(1S)-1-(chloromethyl)-2-phenyleth
yl]-

Synonyms:

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Chemical Property of Benzamide, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis[N-[(1S)-1-(chloromethyl)-2-phenyleth yl]- Edit
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Technology Process of Benzamide, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis[N-[(1S)-1-(chloromethyl)-2-phenyleth yl]-

There total 3 articles about Benzamide, 3,3'-(1,3,4-oxadiazole-2,5-diyl)bis[N-[(1S)-1-(chloromethyl)-2-phenyleth yl]- 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 3 steps
1: SOCl2 / 10 h / Heating
2: 1.24 g / Et3N / CH2Cl2 / 24 h / 20 °C
3: 69 percent / SOCl2 / CH2Cl2 / 5 h / Heating
With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1081/SCC-120021848
Guidance literature:
Multi-step reaction with 2 steps
1: 1.24 g / Et3N / CH2Cl2 / 24 h / 20 °C
2: 69 percent / SOCl2 / CH2Cl2 / 5 h / Heating
With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1081/SCC-120021848
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