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7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate

Base Information Edit
  • Chemical Name:7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate
  • CAS No.:1448297-29-7
  • Molecular Formula:C26H27FN4O5S
  • Molecular Weight:526.589
  • Hs Code.:
  • Mol file:1448297-29-7.mol
7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate

Synonyms:7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate

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Chemical Property of 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate Edit
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Technology Process of 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate

There total 11 articles about 7-[2-((Z)-3-diethylaminoprop-1-enyl)-4-fluorobenzenesulfonyl-amino]-10H-9-oxa-1,2-diazaphenanthrene-8-carboxylate 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 4 steps
1: ammonium formate; palladium 10% on activated carbon / ethanol / 1 h / Reflux; Inert atmosphere
2: sulfuric acid / methanol / 16 h / Reflux
3: dichloromethane; pyridine / 96 h / 20 °C
4: tris-(dibenzylideneacetone)dipalladium(0); tri-tertiary-butyl phosphonium tetrafluoroborate / 1,4-dioxane; dimethyl sulfoxide / 2.25 h / 95 °C / Inert atmosphere
With tris-(dibenzylideneacetone)dipalladium(0); sulfuric acid; palladium 10% on activated carbon; tri-tertiary-butyl phosphonium tetrafluoroborate; ammonium formate; In 1,4-dioxane; pyridine; methanol; ethanol; dichloromethane; dimethyl sulfoxide;
Guidance literature:
Multi-step reaction with 2 steps
1: dichloromethane; pyridine / 96 h / 20 °C
2: tris-(dibenzylideneacetone)dipalladium(0); tri-tertiary-butyl phosphonium tetrafluoroborate / 1,4-dioxane; dimethyl sulfoxide / 2.25 h / 95 °C / Inert atmosphere
With tris-(dibenzylideneacetone)dipalladium(0); tri-tertiary-butyl phosphonium tetrafluoroborate; In 1,4-dioxane; pyridine; dichloromethane; dimethyl sulfoxide;
Guidance literature:
Multi-step reaction with 5 steps
1: trichlorophosphate / 0.75 h / 95 °C
2: ammonium formate; palladium 10% on activated carbon / ethanol / 1 h / Reflux; Inert atmosphere
3: sulfuric acid / methanol / 16 h / Reflux
4: dichloromethane; pyridine / 96 h / 20 °C
5: tris-(dibenzylideneacetone)dipalladium(0); tri-tertiary-butyl phosphonium tetrafluoroborate / 1,4-dioxane; dimethyl sulfoxide / 2.25 h / 95 °C / Inert atmosphere
With tris-(dibenzylideneacetone)dipalladium(0); sulfuric acid; palladium 10% on activated carbon; tri-tertiary-butyl phosphonium tetrafluoroborate; ammonium formate; trichlorophosphate; In 1,4-dioxane; pyridine; methanol; ethanol; dichloromethane; dimethyl sulfoxide;
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