Glycine, N-((2,4-dichlorophenoxy)acetyl)-

Base Information

Chemical Name:Glycine, N-((2,4-dichlorophenoxy)acetyl)-
CAS No.:17212-10-1
Molecular Formula:C₁₀H₉Cl₂NO₄
Molecular Weight:278.092
Hs Code.:2924299090
DSSTox Substance ID:DTXSID60938092
Nikkaji Number:J529.997G
Wikidata:Q82914342
Mol file:17212-10-1.mol

Synonyms:Glycine, N-((2,4-dichlorophenoxy)acetyl)-;17212-10-1;2-[[2-(2,4-dichlorophenoxy)acetyl]amino]acetic acid;Glycine, N-[(2,4-dichlorophenoxy)acetyl]-;n-[(2,4-dichlorophenoxy)acetyl]glycine;AI3-25316;2,4-D Glycine conjugate;DTXSID60938092;ZSUWKPLZWNKGFI-UHFFFAOYSA-N;N-(2.4-Dichlorphenoxyacetyl)-glycin;AKOS002675553;([(2,4-Dichlorophenoxy)acetyl]amino)acetic acid #;Z85886678;N-[2-(2,4-Dichlorophenoxy)-1-hydroxyethylidene]glycine

Suppliers and Price of Glycine, N-((2,4-dichlorophenoxy)acetyl)-

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-((2,4-dichlorophenoxy)acetyl)-

Chemical Property:

Vapor Pressure:6.87E-13mmHg at 25°C
Boiling Point:549.1°Cat760mmHg
Flash Point:285.9°C
PSA：75.63000
Density:1.483g/cm³
LogP:1.96390
XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:276.9908632
Heavy Atom Count:17
Complexity:288

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC(=C(C=C1Cl)Cl)OCC(=O)NCC(=O)O

Technology Process of Glycine, N-((2,4-dichlorophenoxy)acetyl)-

There total 2 articles about Glycine, N-((2,4-dichlorophenoxy)acetyl)- 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:

: 56-40-6,18875-39-3,25718-94-9
glycine

: 774-74-3
2-(2,4-dichlorophenoxy)acetyl chloride

: 17212-10-1
2,4-dichlorophenoxyacetylglycine

Guidance literature:: With sodium hydroxide; benzene;
DOI:10.1021/jo01140a017

Reference yield:

: 17212-10-1
2,4-dichlorophenoxyacetylglycine

Guidance literature:: Glycin, 2,4-D-Cl (2,4-Dichlorphenoxyacetylchlorid);

Reference yield:

: 17212-10-1
2,4-dichlorophenoxyacetylglycine

: 141736-52-9
3-[{4-[1-(2-Chloro-phenyl)-2-(2,4-dichloro-phenoxymethyl)-5-oxo-1,5-dihydro-imidazol-(4E)-ylidenemethyl]-phenyl}-(2-cyano-ethyl)-amino]-propionitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 67 percent / sodium acetate, acetic anhydride / 3 h / Heating

2: 45 percent / 2 h / 160 - 170 °C

With sodium acetate; acetic anhydride;