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2-bromo-N-[2,6-di(propan-2-yl)phenyl]-6,11-dihydrodibenzo[b,e]oxepine-11-carboxamide

Base Information
  • Chemical Name:2-bromo-N-[2,6-di(propan-2-yl)phenyl]-6,11-dihydrodibenzo[b,e]oxepine-11-carboxamide
  • CAS No.:144170-10-5
  • Molecular Formula:C27H28BrNO2
  • Molecular Weight:478.429
  • Hs Code.:
  • Mol file:144170-10-5.mol
2-bromo-N-[2,6-di(propan-2-yl)phenyl]-6,11-dihydrodibenzo[b,e]oxepine-11-carboxamide

Synonyms:2-Bromo-5-nitroanisol;2-Brom-5-nitro-anisol;4-Bromo-3-methoxynitrobenzene;1-bromo-2-methoxy-4-nitro-benzene;Benzene,1-bromo-2-methoxy-4-nitro;2-bromo 5-nitro anisole;

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Chemical Property of 2-bromo-N-[2,6-di(propan-2-yl)phenyl]-6,11-dihydrodibenzo[b,e]oxepine-11-carboxamide
Chemical Property:
  • Vapor Pressure:1.32E-13mmHg at 25°C 
  • Boiling Point:583.6°C at 760 mmHg 
  • Flash Point:306.7°C 
  • PSA:41.82000 
  • Density:1.293g/cm3 
  • LogP:8.00840 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

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Technology Process of 2-bromo-N-[2,6-di(propan-2-yl)phenyl]-6,11-dihydrodibenzo[b,e]oxepine-11-carboxamide

There total 4 articles about 2-bromo-N-[2,6-di(propan-2-yl)phenyl]-6,11-dihydrodibenzo[b,e]oxepine-11-carboxamide 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: 1.) SOCl2 / 1.) CH2Cl2, RT, 17 h, 2.) CH2Cl2, toluen, reflux, 2 h
2: 4.15 g / HCl-AcOH / 24 h / Heating
3: 1.) SOCl2, 2.) NEt3 / 1.) CH2Cl2, 2.) CH2Cl2
With hydrogenchloride; thionyl chloride; acetic acid; triethylamine;
DOI:10.1021/jm00032a014
Guidance literature:
Multi-step reaction with 2 steps
1: 4.15 g / HCl-AcOH / 24 h / Heating
2: 1.) SOCl2, 2.) NEt3 / 1.) CH2Cl2, 2.) CH2Cl2
With hydrogenchloride; thionyl chloride; acetic acid; triethylamine;
DOI:10.1021/jm00032a014
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