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4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine

Base Information Edit
  • Chemical Name:4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine
  • CAS No.:223419-43-0
  • Molecular Formula:C41H36N4O4
  • Molecular Weight:648.761
  • Hs Code.:
  • Mol file:223419-43-0.mol
4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine

Synonyms:4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine

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Chemical Property of 4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine Edit
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Technology Process of 4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine

There total 11 articles about 4-[3-(4,4'-dimethoxytrityloxy)propoxymethyl]-4'-cyano-2,2':6',2-terpyridine 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 9 steps
1.1: potassium tert-butoxide / tetrahydrofuran / 0.17 h / 20 °C
1.2: tetrahydrofuran / 16 h
1.3: 77 percent / ammonium acetate; acetic acid / tetrahydrofuran / 4 h / Heating
2.1: potassium tert-butoxide / dimethylformamide / 1 h / 20 °C
2.2: 82 percent / O2 / dimethylformamide / 6 h
3.1: 77 percent / SOCl2 / 24 h / Heating
4.1: 87 percent / NaBH4 / tetrahydrofuran; ethanol / 8 h / 0 - 80 °C
5.1: 98 percent / NaH / dimethylformamide / 20 °C
6.1: 83 percent / 3-chloroperoxybenzoic acid / CH2Cl2 / 12 h / 20 °C
7.1: 98 percent / Bu4NF / tetrahydrofuran / 3 h / 20 °C
8.1: 91 percent / pyridine; 4-(dimethylamino)pyridine / 30 h / 20 °C
9.1: 89 percent / dimethylformamide / 14 h / 100 °C
With pyridine; dmap; sodium tetrahydroborate; thionyl chloride; potassium tert-butylate; tetrabutyl ammonium fluoride; sodium hydride; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ja048537q
Guidance literature:
Multi-step reaction with 10 steps
1.1: 20 percent / trifluoroacetic acid; aq. tert-butyl hydroperoxide; FeSO4*7H2O / acetonitrile / 4 h / Heating
2.1: potassium tert-butoxide / tetrahydrofuran / 0.17 h / 20 °C
2.2: tetrahydrofuran / 16 h
2.3: 77 percent / ammonium acetate; acetic acid / tetrahydrofuran / 4 h / Heating
3.1: potassium tert-butoxide / dimethylformamide / 1 h / 20 °C
3.2: 82 percent / O2 / dimethylformamide / 6 h
4.1: 77 percent / SOCl2 / 24 h / Heating
5.1: 87 percent / NaBH4 / tetrahydrofuran; ethanol / 8 h / 0 - 80 °C
6.1: 98 percent / NaH / dimethylformamide / 20 °C
7.1: 83 percent / 3-chloroperoxybenzoic acid / CH2Cl2 / 12 h / 20 °C
8.1: 98 percent / Bu4NF / tetrahydrofuran / 3 h / 20 °C
9.1: 91 percent / pyridine; 4-(dimethylamino)pyridine / 30 h / 20 °C
10.1: 89 percent / dimethylformamide / 14 h / 100 °C
With pyridine; tert.-butylhydroperoxide; dmap; sodium tetrahydroborate; thionyl chloride; potassium tert-butylate; tetrabutyl ammonium fluoride; sodium hydride; iron(II) sulfate; 3-chloro-benzenecarboperoxoic acid; trifluoroacetic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1021/ja048537q
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