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2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide

Base Information Edit
  • Chemical Name:2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide
  • CAS No.:66604-68-0
  • Molecular Formula:C18H17N2+
  • Molecular Weight:388.251
  • Hs Code.:
  • Mol file:66604-68-0.mol
2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide

Synonyms:

Suppliers and Price of 2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 5 raw suppliers
Chemical Property of 2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide Edit
Chemical Property:
  • Vapor Pressure:1.3E-09mmHg at 25°C 
  • Boiling Point:°Cat760mmHg 
  • Flash Point:°C 
  • Density:g/cm3 
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide

There total 7 articles about 2,5,11-trimethyl-5a,6-dihydro-2H-pyrido[4,3-b]carbazol-6-ium iodide 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:
2-methyl-5-methoxycarbonyl-11-methyl-6H-pyrido[4,3-b]carbazol-2-ium iodide; With sodium bis(2-methoxyethoxy)aluminium dihydride; In 5,5-dimethyl-1,3-cyclohexadiene; toluene; at 130 ℃; for 6h;
With 3-ethoxycarbonyl-1-methylpyridinium chloride; In methanol; at 20 ℃; for 5h;
DOI:10.1016/j.ejmech.2014.05.032
Guidance literature:
Multi-step reaction with 5 steps
1.1: toluene-4-sulfonic acid / ethanol / 1.5 h / Reflux
2.1: trichlorophosphate / 1,2-dichloro-benzene / 1.5 h / 20 °C
2.2: 4 h / 105 °C
2.3: 20 °C
3.1: 3 h / 115 °C / Inert atmosphere
3.2: 1 h / 20 °C / Molecular sieve; Inert atmosphere
4.1: sodium carbonate; p-toluenesulfonyl chloride / tetrahydrofuran; water / 2 h / 20 °C
4.2: 12 h
4.3: 0 °C / pH 10
5.1: acetone / 48 h / Darkness
With sodium carbonate; toluene-4-sulfonic acid; p-toluenesulfonyl chloride; trichlorophosphate; In tetrahydrofuran; ethanol; water; 1,2-dichloro-benzene; acetone; 2.1: Vilsmeier-Haack reaction / 2.2: Vilsmeier-Haack reaction;
DOI:10.1016/j.bmc.2011.07.020
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