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Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester

Base Information Edit
  • Chemical Name:Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester
  • CAS No.:159871-51-9
  • Molecular Formula:C8H15NO2
  • Molecular Weight:157.213
  • Hs Code.:
  • Mol file:159871-51-9.mol
Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester

Synonyms:

Suppliers and Price of Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester
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
  • Acrotein
  • tert-Butyl1-aminocyclopropanecarboxylate 97%
  • 5g
  • $ 990.00
  • Acrotein
  • tert-Butyl1-aminocyclopropanecarboxylate 97%
  • 1g
  • $ 339.17
Total 4 raw suppliers
Chemical Property of Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester Edit
Chemical Property:
  • Boiling Point:190.2±23.0 °C(Predicted) 
  • PKA:6.40±0.20(Predicted) 
  • PSA:0.00000 
  • Density:1.073±0.06 g/cm3(Predicted) 
  • LogP:0.00000 
Purity/Quality:

97% *data from raw suppliers

tert-Butyl1-aminocyclopropanecarboxylate 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester

There total 4 articles about Cyclopropanecarboxylic acid, 1-amino-, 1,1-dimethylethyl ester 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 hydrogen; palladium 10% on activated carbon; In methanol; for 3h;
Guidance literature:
Multi-step reaction with 4 steps
1.1: potassium carbonate / N,N-dimethyl-formamide / 20 °C
2.1: sodium hydroxide / ethanol
3.1: triethylamine; diphenyl phosphoryl azide / dichloromethane / 2 h / Inert atmosphere; Reflux
3.2: 5 h / Reflux
4.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 6 h / 20 °C
With diphenyl phosphoryl azide; palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/acsmedchemlett.7b00544
Guidance literature:
Multi-step reaction with 3 steps
1.1: sodium hydroxide / ethanol
2.1: triethylamine; diphenyl phosphoryl azide / dichloromethane / 2 h / Inert atmosphere; Reflux
2.2: 5 h / Reflux
3.1: palladium 10% on activated carbon; hydrogen / tetrahydrofuran; methanol / 6 h / 20 °C
With diphenyl phosphoryl azide; palladium 10% on activated carbon; hydrogen; triethylamine; sodium hydroxide; In tetrahydrofuran; methanol; ethanol; dichloromethane;
DOI:10.1021/acsmedchemlett.7b00544
Refernces Edit
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