Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)-

Base Information

Chemical Name:Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)-
CAS No.:49808-81-3
Molecular Formula:C₁₀H₁₂Cl₂N₂O₂
Molecular Weight:263.123
Hs Code.:
DSSTox Substance ID:DTXSID50484710

Synonyms:49808-81-3;Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)-;DTXSID50484710

Suppliers and Price of Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)-

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 Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)-

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:262.0275830
Heavy Atom Count:16
Complexity:229

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)-

There total 2 articles about Acetamide, N-(2-aminoethyl)-2-(2,4-dichlorophenoxy)- 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:

: 94-75-7,89300-30-1
2,4-Dichlorophenoxyacetic acid

: 107-15-3,85404-18-8
ethylenediamine

: 49808-81-3
N-(2.4-Dichlor-phenoxyacetyl)-aethylendiamin

Guidance literature:: Multistep reaction.;
DOI:10.1021/ac011051x

Reference yield:

: 49808-81-3
N-(2.4-Dichlor-phenoxyacetyl)-aethylendiamin

Guidance literature:: 2.4-Dichlorphenoxy-essigsaeure-cyanmethylester, Aethylendiamin/Me.;

Reference yield:

: 49808-81-3
N-(2.4-Dichlor-phenoxyacetyl)-aethylendiamin

: Cl₂C₆H₃OCH₂CONHCH₂CH₂NHCOCH(CH₂CH₂CH₂CH₂NHC₂₁H₁₀NO₄S)NHC₂₁H₁₀NO₄S

Guidance literature:: Multi-step reaction with 2 steps

1.1: dicyclohexyl carbodiimide; hydroxybenzotriazole / 24 h

1.2: isopropylamine / CH₂Cl₂ / 0.5 h

2.1: diisopropylethylamine / methanol

With benzotriazol-1-ol; N-ethyl-N,N-diisopropylamine; dicyclohexyl-carbodiimide; In methanol;
DOI:10.1021/ac011051x