Glycine, N-(4-ethoxyphenyl)-

Base Information

Chemical Name:Glycine, N-(4-ethoxyphenyl)-
CAS No.:67870-18-2
Molecular Formula:C₁₀H₁₃NO₃
Molecular Weight:195.218
Hs Code.:
DSSTox Substance ID:DTXSID50396546
Wikidata:Q82197312

Synonyms:Glycine, N-(4-ethoxyphenyl)-;67870-18-2;2-[(4-ethoxyphenyl)amino]acetic Acid;2-(4-ethoxyanilino)acetic acid;4-ethoxyphenyl-glycine;N-(4-ethoxyphenyl)glycine;Oprea1_231419;SCHEMBL2454762;DTXSID50396546;STL583880;AKOS000101473

Suppliers and Price of Glycine, N-(4-ethoxyphenyl)-

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 Glycine, N-(4-ethoxyphenyl)-

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:195.08954328
Heavy Atom Count:14
Complexity:176

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC1=CC=C(C=C1)NCC(=O)O

Technology Process of Glycine, N-(4-ethoxyphenyl)-

There total 1 articles about Glycine, N-(4-ethoxyphenyl)- 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:

: 79-11-8
chloroacetic acid

: 156-43-4
4-Ethoxyaniline

: 67870-18-2
N-(4-ethoxy-phenyl)-glycine

Guidance literature:: With sodium hydroxide; water;

Reference yield:

: 20423-52-3
3-chloro-1-methyl-3-phenyl-1,3-dihydroindol-2-one

: 67870-18-2
N-(4-ethoxy-phenyl)-glycine

: C₂₄H₂₄N₂O₂

: C₂₄H₂₄N₂O₂

Guidance literature:: With 5,6-bis(5-methoxythiophen-2-yl)pyrazine-2,3-dicarbonitrile; C₆₇H₄₇O₄P; potassium hydrogencarbonate; In tetrahydrofuran; tert-butyl methyl ether; at -40 ℃; for 24h; enantioselective reaction; Irradiation;
DOI:10.1039/c9cc05304b