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(2,6-(2,4,6-Me3C6H2)2C6H3)(2-(2,4,6-Me3C6H2)C6H4)N3H

Base Information
  • Chemical Name:(2,6-(2,4,6-Me3C6H2)2C6H3)(2-(2,4,6-Me3C6H2)C6H4)N3H
  • CAS No.:869383-21-1
  • Molecular Formula:C39H41N3
  • Molecular Weight:551.775
  • Hs Code.:
(2,6-(2,4,6-Me<sub>3</sub>C<sub>6</sub>H<sub>2</sub>)2C<sub>6</sub>H<sub>3</sub>)(2-(2,4,6-Me<sub>3</sub>C<sub>6</sub>H<sub>2</sub>)C<sub>6</sub>H<sub>4</sub>)N<sub>3</sub>H

Synonyms:(2,6-(2,4,6-Me3C6H2)2C6H3)(2-(2,4,6-Me3C6H2)C6H4)N3H

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Chemical Property of (2,6-(2,4,6-Me3C6H2)2C6H3)(2-(2,4,6-Me3C6H2)C6H4)N3H
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Technology Process of (2,6-(2,4,6-Me3C6H2)2C6H3)(2-(2,4,6-Me3C6H2)C6H4)N3H

There total 1 articles about (2,6-(2,4,6-Me3C6H2)2C6H3)(2-(2,4,6-Me3C6H2)C6H4)N3H 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:
1-iodo-2-(2′,4′,6′-trimethylphenyl)benzene; With n-butyllithium; In diethyl ether; hexane; cooling;
2'-azido-2,4,6,2'',4'',6''-hexamethyl-[1,1';3',1'']terphenyl; In diethyl ether; hexane;
DOI:10.1002/anie.200501494
Guidance literature:
In n-heptane; toluene; under Ar atm. TlOEt was added at 0°C to soln. ligand in n-heptane- toluene (4:1), stirred for 30 min, and heated to 80°C; afrer centrifugation soln. was kept overnight at room temp.; elem. anal.;
DOI:10.1021/ic800029z
Guidance literature:
With nBuLi; In diethyl ether; hexane; byproducts: LiBr, nBuH; under Ar, using Schlenk technique; to stirred cooled soln. of triazene deriv. in ethyl ether added n-BuLi in hexane; stirred for 30 min; HgCl2 added, stirred at ambient temp. for 4 h; volatile materials removed under reduced pressure; solid extd. with n-heptane; LiBr separated by centrifugation, filtrate concd., cooled at -20°C;
DOI:10.1002/zaac.200900482
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