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7-benzyl-7H-benzo[e]pyrido[3,2-b]indole

Base Information
  • Chemical Name:7-benzyl-7H-benzo[e]pyrido[3,2-b]indole
  • CAS No.:1520093-73-5
  • Molecular Formula:C22H16N2
  • Molecular Weight:308.382
  • Hs Code.:
7-benzyl-7H-benzo[e]pyrido[3,2-b]indole

Synonyms:7-benzyl-7H-benzo[e]pyrido[3,2-b]indole

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Chemical Property of 7-benzyl-7H-benzo[e]pyrido[3,2-b]indole
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Technology Process of 7-benzyl-7H-benzo[e]pyrido[3,2-b]indole

There total 6 articles about 7-benzyl-7H-benzo[e]pyrido[3,2-b]indole 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:
C15H10INO; With trifluorormethanesulfonic acid; In dichloromethane; at 0 ℃; for 1h; Inert atmosphere;
benzylamine; With tris-(dibenzylideneacetone)dipalladium(0); 4,5’-bis(diphenylphosphino)-9,9’-dimethylxanthene; caesium carbonate; In dichloromethane; toluene; at 110 ℃; for 0.0833333h; Inert atmosphere;
DOI:10.1055/s-0033-1338530
Guidance literature:
Multi-step reaction with 5 steps
1.1: triphenylphosphine; sodium carbonate; palladium 10% on activated carbon / 1,2-dimethoxyethane; water / 16 h / 80 °C / Inert atmosphere
2.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 16 h
3.1: toluene-4-sulfonic acid; sodium nitrite; potassium iodide / water; acetonitrile / 1 h / 10 - 15 °C / Inert atmosphere
4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.17 h / 0 °C / Inert atmosphere; Sealed tube
5.1: trifluorormethanesulfonic acid / dichloromethane / 1 h / 0 °C / Inert atmosphere
5.2: 0.08 h / 110 °C / Inert atmosphere
With trifluorormethanesulfonic acid; palladium 10% on activated carbon; hydrogen; sodium carbonate; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; potassium iodide; sodium nitrite; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water; acetonitrile; 1.1: |Suzuki Coupling / 3.1: |Sandmeyer Reaction / 5.2: |Buchwald-Hartwig Coupling;
DOI:10.1055/s-0033-1338530
Guidance literature:
Multi-step reaction with 5 steps
1.1: triphenylphosphine; sodium carbonate; palladium 10% on activated carbon / 1,2-dimethoxyethane; water / 16 h / 80 °C / Inert atmosphere
2.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran / 16 h
3.1: toluene-4-sulfonic acid; sodium nitrite; potassium iodide / water; acetonitrile / 1 h / 10 - 15 °C / Inert atmosphere
4.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.17 h / 0 °C / Inert atmosphere; Sealed tube
5.1: trifluorormethanesulfonic acid / dichloromethane / 1 h / 0 °C / Inert atmosphere
5.2: 0.08 h / 110 °C / Inert atmosphere
With trifluorormethanesulfonic acid; palladium 10% on activated carbon; hydrogen; sodium carbonate; toluene-4-sulfonic acid; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; potassium iodide; sodium nitrite; In tetrahydrofuran; 1,2-dimethoxyethane; dichloromethane; water; acetonitrile; 1.1: |Suzuki Coupling / 3.1: |Sandmeyer Reaction / 5.2: |Buchwald-Hartwig Coupling;
DOI:10.1055/s-0033-1338530
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