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3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid

Base Information Edit
  • Chemical Name:3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid
  • CAS No.:1427319-48-9
  • Molecular Formula:C11H19NO4
  • Molecular Weight:229.276
  • Hs Code.:
  • Mol file:1427319-48-9.mol
3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid

Synonyms:

Suppliers and Price of 3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid
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
  • ACHEMBLOCK
  • (1s,3s)-3-(((tert-butoxycarbonyl)amino)methyl)cyclobutane-1-carboxylicacid 97%
  • 100MG
  • $ 215.00
Total 4 raw suppliers
Chemical Property of 3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid Edit
Chemical Property:
Purity/Quality:

99%, *data from raw suppliers

(1s,3s)-3-(((tert-butoxycarbonyl)amino)methyl)cyclobutane-1-carboxylicacid 97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid

There total 7 articles about 3-(((tert-butoxycarbonyl)amino)methyl)cyclobutanecarboxylic acid 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:
cis-3-(aminomethyl)cyclobutanecarboxylic acid hydrochloride; With sodium hydroxide; In 1,4-dioxane; water; for 0.166667h;
di-tert-butyl dicarbonate; In 1,4-dioxane; water; for 3h; Inert atmosphere;
DOI:10.1007/s00726-012-1362-3
Guidance literature:
Multi-step reaction with 5 steps
1.1: triethylamine; methanesulfonyl chloride / dichloromethane / 16 h / -10 - 20 °C / Inert atmosphere
1.2: 24 h / Inert atmosphere; Reflux
2.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -20 °C / Inert atmosphere
3.1: ammonia; lithium / tetrahydrofuran; tert-butyl alcohol / -78 °C / Inert atmosphere
4.1: hydrogenchloride / water / Inert atmosphere
5.1: sodium hydroxide / water; 1,4-dioxane / 0.17 h
5.2: 3 h / Inert atmosphere
With hydrogenchloride; ammonia; lithium; methanesulfonyl chloride; triethylamine; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; dichloromethane; water; tert-butyl alcohol;
DOI:10.1007/s00726-012-1362-3
Guidance literature:
Multi-step reaction with 7 steps
1.1: hydrogen; palladium on activated charcoal; sodium carbonate / ethanol / 12 h / 20 °C
2.1: lithium borohydride / tetrahydrofuran / 12 h / 20 °C / Inert atmosphere
3.1: triethylamine; methanesulfonyl chloride / dichloromethane / 16 h / -10 - 20 °C / Inert atmosphere
3.2: 24 h / Inert atmosphere; Reflux
4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -20 °C / Inert atmosphere
5.1: ammonia; lithium / tetrahydrofuran; tert-butyl alcohol / -78 °C / Inert atmosphere
6.1: hydrogenchloride / water / Inert atmosphere
7.1: sodium hydroxide / water; 1,4-dioxane / 0.17 h
7.2: 3 h / Inert atmosphere
With hydrogenchloride; lithium borohydride; palladium on activated charcoal; ammonia; hydrogen; lithium; sodium carbonate; methanesulfonyl chloride; triethylamine; sodium hydroxide; lithium hexamethyldisilazane; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; tert-butyl alcohol;
DOI:10.1007/s00726-012-1362-3
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