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C27H28Cl2N6O5S

Base Information
  • Chemical Name:C27H28Cl2N6O5S
  • CAS No.:1365992-37-5
  • Molecular Formula:C27H28Cl2N6O5S
  • Molecular Weight:619.529
  • Hs Code.:
C<sub>27</sub>H<sub>28</sub>Cl<sub>2</sub>N<sub>6</sub>O<sub>5</sub>S

Synonyms:C27H28Cl2N6O5S

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Chemical Property of C27H28Cl2N6O5S
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Technology Process of C27H28Cl2N6O5S

There total 12 articles about C27H28Cl2N6O5S 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: diphenyl phosphoryl azide / toluene / 3 h / 110 °C / Inert atmosphere
2.1: trifluoroacetic acid / dichloromethane / 5 h / 20 °C
2.2: NH2 cartridge
3.1: triethylamine / 1,4-dioxane / 18 h / 100 °C
4.1: thionyl chloride / 56 h / 90 °C
5.1: thiourea; pyridine / isopropyl alcohol / 3.5 h / 90 °C
5.2: 1.5 h / 90 °C
6.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 2 h / 100 °C / Inert atmosphere
7.1: ozone / dichloromethane; methanol / 0.17 h / -78 °C
7.2: -78 - 20 °C / Inert atmosphere
8.1: sodium cyanoborohydride; acetic acid / dichloromethane; methanol / 2 h
9.1: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium(0) / 1,4-dioxane / 5 h / 80 °C / Inert atmosphere
With pyridine; thionyl chloride; diphenyl phosphoryl azide; sodium cyanoborohydride; sodium carbonate; caesium carbonate; ozone; acetic acid; triethylamine; thiourea; trifluoroacetic acid; bis-triphenylphosphine-palladium(II) chloride; tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; methanol; dichloromethane; water; isopropyl alcohol; toluene;
Guidance literature:
Multi-step reaction with 3 steps
1: sodium azide / 4 h / 70 °C
2: hydrogen / 5%-palladium/activated carbon / ethyl acetate; industrial methylated spirits / 18 h / 20 °C
3: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium(0) / 1,4-dioxane / 5 h / 80 °C / Inert atmosphere
With sodium azide; hydrogen; caesium carbonate; tris-(dibenzylideneacetone)dipalladium(0); 5%-palladium/activated carbon; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; industrial methylated spirits; ethyl acetate;
Guidance literature:
Multi-step reaction with 8 steps
1.1: thionyl chloride / 2 h / Reflux
2.1: triethylamine / 1,4-dioxane / 18 h / 100 °C
3.1: thionyl chloride / 56 h / 90 °C
4.1: thiourea; pyridine / isopropyl alcohol / 3.5 h / 90 °C
4.2: 1.5 h / 90 °C
5.1: sodium carbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 2 h / 100 °C / Inert atmosphere
6.1: ozone / dichloromethane; methanol / 0.17 h / -78 °C
6.2: -78 - 20 °C / Inert atmosphere
7.1: sodium cyanoborohydride; acetic acid / dichloromethane; methanol / 2 h
8.1: caesium carbonate / 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium(0) / 1,4-dioxane / 5 h / 80 °C / Inert atmosphere
With pyridine; thionyl chloride; sodium cyanoborohydride; sodium carbonate; caesium carbonate; ozone; acetic acid; triethylamine; thiourea; bis-triphenylphosphine-palladium(II) chloride; tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; In 1,4-dioxane; methanol; dichloromethane; water; isopropyl alcohol;
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