Tert-butyl 2-(tert-butylamino)acetate

Base Information

Chemical Name:Tert-butyl 2-(tert-butylamino)acetate
CAS No.:916885-51-3
Molecular Formula:C₁₀H₂₁NO₂
Molecular Weight:187.282
Hs Code.:
DSSTox Substance ID:DTXSID10427224
Nikkaji Number:J2.390.894H
Wikidata:Q82239924
Mol file:916885-51-3.mol

Synonyms:Tert-butyl 2-(tert-butylamino)acetate;916885-51-3;N-t-butylglycine tert-butyl ester;tert-Butyl tert-butylglycinate;SCHEMBL756932;AMY4143;DTXSID10427224;N-tert-Butylglycine tert-butyl ester;CS-0249086;FT-0699212;EN300-4243516

Suppliers and Price of Tert-butyl 2-(tert-butylamino)acetate

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 5 raw suppliers

Chemical Property of Tert-butyl 2-(tert-butylamino)acetate

Chemical Property:

PSA：38.33000
LogP:2.10710
XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:187.157228913
Heavy Atom Count:13
Complexity:174

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)NCC(=O)OC(C)(C)C

Technology Process of Tert-butyl 2-(tert-butylamino)acetate

There total 1 articles about Tert-butyl 2-(tert-butylamino)acetate 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: 75.0%

: 5292-43-3
bromoacetic acid tert-butyl ester

: 75-64-9
tert-butylamine

: 916885-51-3
(tert-butylamino)acetic acid tert-butyl ester

Guidance literature:: In tetrahydrofuran; at 0 - 20 ℃;
DOI:10.1021/ol062126s

Reference yield:

: 916885-51-3
(tert-butylamino)acetic acid tert-butyl ester

: 2-tert-butylaminoacetylchloride hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: water; hydrogenchloride

2: thionyl chloride

With hydrogenchloride; thionyl chloride; water;
DOI:10.1016/j.tetlet.2020.152126