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(2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine

Base Information Edit
  • Chemical Name:(2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine
  • CAS No.:405891-90-9
  • Molecular Formula:C19H20N2O3S
  • Molecular Weight:356.445
  • Hs Code.:
  • Mol file:405891-90-9.mol
(2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine

Synonyms:(2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine

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Chemical Property of (2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine Edit
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Technology Process of (2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine

There total 10 articles about (2-benzenesulfonyl-2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)dimethylamine 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:
dimethyl-(2,7,8,9-tetrahydro-6-oxa-2-azabenzo[c,d]azulen-8-yl)amine; With n-butyllithium; In tetrahydrofuran; hexane; chloroform; at -70 - -30 ℃; for 2h;
benzenesulfonyl chloride; In tetrahydrofuran; hexane; at -70 - 20 ℃;
Guidance literature:
Multi-step reaction with 10 steps
1.1: trichlorophosphate / 2 h / 20 °C
1.2: 0.25 h
2.1: dmap / acetonitrile / 3 h / 0 °C
3.1: 1,4-diaza-bicyclo[2.2.2]octane / 24 h / 4 °C
4.1: pyridine; acetic anhydride / 1 h / 0 °C
4.2: 6 h / 80 °C
5.1: sodium hydroxide / tetrahydrofuran; water / 1 h
5.2: 3 h / 50 °C
6.1: chloroformic acid ethyl ester; triethylamine / tetrahydrofuran / 0.5 h / 0 °C
6.2: 4 h / 0 °C
7.1: 1,4-dioxane / 0.33 h / Heating / reflux
8.1: hydrogenchloride / 1,4-dioxane; water / 0.33 h / Heating / reflux
9.1: sodium tris(acetoxy)borohydride; acetic acid / tetrahydrofuran / 1 h / 20 °C
10.1: n-butyllithium / tetrahydrofuran; hexane; chloroform / 2 h / -70 - -30 °C
10.2: -70 - 20 °C
With pyridine; 1,4-diaza-bicyclo[2.2.2]octane; hydrogenchloride; dmap; sodium hydroxide; n-butyllithium; chloroformic acid ethyl ester; acetic anhydride; sodium tris(acetoxy)borohydride; acetic acid; triethylamine; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; hexane; chloroform; water; acetonitrile;
Guidance literature:
Multi-step reaction with 7 steps
1.1: sodium hydride / tetrahydrofuran / 19 h / 0 °C
2.1: sodium hydroxide / tetrahydrofuran; water / 1 h
2.2: 3 h / 50 °C
3.1: chloroformic acid ethyl ester; triethylamine / tetrahydrofuran / 0.5 h / 0 °C
3.2: 4 h / 0 °C
4.1: 1,4-dioxane / 0.33 h / Heating / reflux
5.1: hydrogenchloride / 1,4-dioxane; water / 0.33 h / Heating / reflux
6.1: sodium tris(acetoxy)borohydride; acetic acid / tetrahydrofuran / 1 h / 20 °C
7.1: n-butyllithium / tetrahydrofuran; hexane; chloroform / 2 h / -70 - -30 °C
7.2: -70 - 20 °C
With hydrogenchloride; sodium hydroxide; n-butyllithium; chloroformic acid ethyl ester; sodium tris(acetoxy)borohydride; sodium hydride; acetic acid; triethylamine; In tetrahydrofuran; 1,4-dioxane; hexane; chloroform; water;
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