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3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic acid

Base Information Edit
  • Chemical Name:3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic acid
  • CAS No.:372144-22-4
  • Molecular Formula:C13H18N2O4
  • Molecular Weight:266.297
  • Hs Code.:
  • Mol file:372144-22-4.mol
3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic acid

Synonyms:3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic acid;3-(2-PYRIDYL)-3-(BOC-AMINO)PROPIONIC ACID

Suppliers and Price of 3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic 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
  • American Custom Chemicals Corporation
  • 3-[(TERT-BUTOXYCARBONYL)AMINO]-3-PYRIDIN-2-YLPROPANOIC ACID 95.00%
  • 5MG
  • $ 505.48
Total 1 raw suppliers
Chemical Property of 3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic acid Edit
Chemical Property:
Purity/Quality:

3-[(TERT-BUTOXYCARBONYL)AMINO]-3-PYRIDIN-2-YLPROPANOIC ACID 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
Technology Process of 3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic acid

There total 5 articles about 3-[(tert-butoxycarbonyl)amino]-3-pyridin-2-ylpropanoic 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:
With water; lithium hydroxide; In tetrahydrofuran; methanol; at 20 ℃;
Guidance literature:
Multi-step reaction with 5 steps
1.1: titanium(IV) tetraethanolate / tetrahydrofuran / 80 °C
2.1: lithium diisopropyl amide / tetrahydrofuran; tert-butyl methyl ether / 1.5 h / -78 °C / Inert atmosphere
2.2: 3.5 h / -78 °C
3.1: hydrogenchloride / 1,4-dioxane / 8 h / 0 - 20 °C
4.1: sodium hydrogencarbonate / 1,4-dioxane / 16 h / 20 °C
5.1: lithium hydroxide; water / methanol; tetrahydrofuran / 20 °C
With hydrogenchloride; titanium(IV) tetraethanolate; water; sodium hydrogencarbonate; lithium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; methanol; tert-butyl methyl ether;
Guidance literature:
Multi-step reaction with 4 steps
1.1: lithium diisopropyl amide / tetrahydrofuran; tert-butyl methyl ether / 1.5 h / -78 °C / Inert atmosphere
1.2: 3.5 h / -78 °C
2.1: hydrogenchloride / 1,4-dioxane / 8 h / 0 - 20 °C
3.1: sodium hydrogencarbonate / 1,4-dioxane / 16 h / 20 °C
4.1: lithium hydroxide; water / methanol; tetrahydrofuran / 20 °C
With hydrogenchloride; water; sodium hydrogencarbonate; lithium hydroxide; lithium diisopropyl amide; In tetrahydrofuran; 1,4-dioxane; methanol; tert-butyl methyl ether;
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