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2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane

Base Information Edit
  • Chemical Name:2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane
  • CAS No.:1032903-51-7
  • Molecular Formula:C16H24BNO5
  • Molecular Weight:321.181
  • Hs Code.:
  • Mol file:1032903-51-7.mol
2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane

Synonyms:2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane

Suppliers and Price of 2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 2 raw suppliers
Chemical Property of 2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

Safty Information:
  • Pictogram(s):  
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MSDS Files:
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Technology Process of 2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane

There total 4 articles about 2-(5-isopropoxy-2-methyl-4-nitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxide cyclopentaborane 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:
With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium acetate; In dimethyl sulfoxide; at 85 ℃; for 18h; Inert atmosphere;
Guidance literature:
With tris-(dibenzylideneacetone)dipalladium(0); potassium acetate; tricyclohexylphosphine; In 1,4-dioxane; at 100 ℃; for 24.1h;
Guidance literature:
Multi-step reaction with 3 steps
1: sulfuric acid; potassium nitrate / 22 h / 0 - 20 °C
2: caesium carbonate / 24 h / 60 °C
3: tricyclohexylphosphine; tris-(dibenzylideneacetone)dipalladium(0); potassium acetate / 1,4-dioxane / 24.1 h / 100 °C
With tris-(dibenzylideneacetone)dipalladium(0); sulfuric acid; potassium acetate; caesium carbonate; potassium nitrate; tricyclohexylphosphine; In 1,4-dioxane;
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