N-tert-Butyl-N-(4-nitrobenzoyl)glycine

Base Information

Chemical Name:N-tert-Butyl-N-(4-nitrobenzoyl)glycine
CAS No.:143159-79-9
Molecular Formula:C13H16N2O5
Molecular Weight:280.28
Hs Code.:
DSSTox Substance ID:DTXSID20569669
Wikidata:Q82456870

Synonyms:143159-79-9;N-tert-Butyl-N-(4-nitrobenzoyl)glycine;DTXSID20569669;AKOS017818384

Suppliers and Price of N-tert-Butyl-N-(4-nitrobenzoyl)glycine

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 1 raw suppliers

Chemical Property of N-tert-Butyl-N-(4-nitrobenzoyl)glycine

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:4
Exact Mass:280.10592162
Heavy Atom Count:20
Complexity:389

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)N(CC(=O)O)C(=O)C1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of N-tert-Butyl-N-(4-nitrobenzoyl)glycine

There total 3 articles about N-tert-Butyl-N-(4-nitrobenzoyl)glycine 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: 87.0%

: 143159-80-2
N-(1,1-Dimethylethyl)-N-(4-nitrobenzoyl)-aminoacetic acid ethyl ester

: 143159-79-9
N-(1,1-Dimethylethyl)-N-(4-nitrobenzoyl)-aminoacetic acid

Guidance literature:: With sodium hydroxide; for 2h; Heating;

Reference yield:

: 37885-76-0
ethyl 2-(tert-butylamino)acetate

: 143159-79-9
N-(1,1-Dimethylethyl)-N-(4-nitrobenzoyl)-aminoacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / pyridine / 1 h / 20 °C

2: 87 percent / 10 percent aq. NaOH / 2 h / Heating

With pyridine; sodium hydroxide; 1: Acylation / 2: Hydrolysis;

Reference yield:

: 122-04-3
4-nitro-benzoyl chloride

: 143159-79-9
N-(1,1-Dimethylethyl)-N-(4-nitrobenzoyl)-aminoacetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / pyridine / 1 h / 20 °C

2: 87 percent / 10 percent aq. NaOH / 2 h / Heating

With pyridine; sodium hydroxide; 1: Acylation / 2: Hydrolysis;