Tert-butyl 2-aminopentanoate

Base Information

Chemical Name:Tert-butyl 2-aminopentanoate
CAS No.:17389-07-0
Molecular Formula:C₉H₁₉NO₂
Molecular Weight:173.255
Hs Code.:
European Community (EC) Number:837-366-3

Synonyms:tert-butyl 2-aminopentanoate;17389-07-0;tert-butyl2-aminopentanoate;SCHEMBL67350;tert-butyl 4-methyl-aminobutyrate;SGGQAQREPOYSME-UHFFFAOYSA-N;tert-Butyl (S)-2-aminopentanoate;AKOS010133872;EN300-135460;A809999;Z600614600

Suppliers and Price of Tert-butyl 2-aminopentanoate

Supply Marketing:

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 3 raw suppliers

Chemical Property of Tert-butyl 2-aminopentanoate

Chemical Property:

XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:173.141578849
Heavy Atom Count:12
Complexity:149

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCC(C(=O)OC(C)(C)C)N

Technology Process of Tert-butyl 2-aminopentanoate

There total 2 articles about Tert-butyl 2-aminopentanoate 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:

Reference yield:

: 64923-12-2
tert-butyl N-benzylideneglycinate

: 106-94-5
propyl bromide

: 17389-07-0,158741-16-3
2-amino-pentanoic acid tert.butyl ester

Guidance literature:: tert-butyl N-benzylideneglycinate; propyl bromide; With N,N,N,N,N,N-hexamethylphosphoric triamide; lithium diisopropyl amide; In tetrahydrofuran; at -78 - 20 ℃; for 12.5h; Schlenk technique; Inert atmosphere;

With hydrogenchloride; In diethyl ether; at 20 ℃; for 4h;
DOI:10.1002/cjoc.202100002