Welcome to LookChem.com Sign In|Join Free
  • or

Encyclopedia

(1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt

Base Information Edit
  • Chemical Name:(1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt
  • CAS No.:1283716-39-1
  • Molecular Formula:C10H14O4*C14H15N
  • Molecular Weight:395.499
  • Hs Code.:
  • Mol file:1283716-39-1.mol
(1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt

Synonyms:(1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt

Suppliers and Price of (1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 0 raw suppliers
Chemical Property of (1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt Edit
Chemical Property:
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of (1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt

There total 4 articles about (1S,2S)-2-vinylcyclopropane-1,1-dicarboxylic acid isopropyl ester dibenzylamine salt 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:
(S)-2-vinyl-cyclopropane-1,1-dicarboxylic acid diisopropyl ester; With tetramethyl ammoniumhydroxide; In water; isopropyl alcohol; at 40 ℃; for 6h;
dibenzylamine; In water; isopropyl alcohol; for 0.5h; Cooling with ice;
Guidance literature:
Multi-step reaction with 7 steps
1.1: hydrogen; 10 wt% Pd(OH)2 on carbon / tetrahydrofuran; isopropyl alcohol / 20 °C
2.1: triethylamine / dichloromethane / 1 h / 20 °C / Cooling with ice
3.1: sodium hydride / N,N-dimethyl-formamide; paraffin oil / 1 h / 20 °C / Inert atmosphere; Cooling with ice
4.1: sodium hydride / methanol / 20 °C
5.1: triethylamine / dichloromethane / 2.5 h / 20 °C / Cooling with ice
6.1: sodium iodide; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 4.5 h / 80 °C
7.1: tetramethyl ammoniumhydroxide / water; isopropyl alcohol / 6 h / 40 °C
7.2: 0.5 h / Cooling with ice
With 10 wt% Pd(OH)2 on carbon; tetramethyl ammoniumhydroxide; hydrogen; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; sodium iodide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol; paraffin oil;
Guidance literature:
Multi-step reaction with 6 steps
1.1: triethylamine / dichloromethane / 1 h / 20 °C / Cooling with ice
2.1: sodium hydride / N,N-dimethyl-formamide; paraffin oil / 1 h / 20 °C / Inert atmosphere; Cooling with ice
3.1: sodium hydride / methanol / 20 °C
4.1: triethylamine / dichloromethane / 2.5 h / 20 °C / Cooling with ice
5.1: sodium iodide; tetra-(n-butyl)ammonium iodide / N,N-dimethyl-formamide / 4.5 h / 80 °C
6.1: tetramethyl ammoniumhydroxide / water; isopropyl alcohol / 6 h / 40 °C
6.2: 0.5 h / Cooling with ice
With tetramethyl ammoniumhydroxide; tetra-(n-butyl)ammonium iodide; sodium hydride; triethylamine; sodium iodide; In methanol; dichloromethane; water; N,N-dimethyl-formamide; isopropyl alcohol; paraffin oil;
Post RFQ for Price