Benzeneacetamide, N-[2-[[2-hydroxy-3-(2-phenoxye

Base Information

Chemical Name:Benzeneacetamide, N-[2-[[2-hydroxy-3-(2-phenoxye
CAS No.:121508-95-0
Molecular Formula:C₂₁H₂₈N₂O₄
Molecular Weight:372.464
Hs Code.:
DSSTox Substance ID:DTXSID30875329
Nikkaji Number:J1.562.006D

Synonyms:121508-95-0;BENZENEACETAMIDE, N-[2-[[2-HYDROXY-3-(2-PHENOXYE;DTXSID30875329

Suppliers and Price of Benzeneacetamide, N-[2-[[2-hydroxy-3-(2-phenoxye

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzeneacetamide, N-[2-[[2-hydroxy-3-(2-phenoxye

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:13
Exact Mass:372.20490738
Heavy Atom Count:27
Complexity:382

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC(=O)NCCNCC(COCCOC2=CC=CC=C2)O

Technology Process of Benzeneacetamide, N-[2-[[2-hydroxy-3-(2-phenoxye

There total 2 articles about Benzeneacetamide, N-[2-[[2-hydroxy-3-(2-phenoxye 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: 44.0%

: 15070-17-4
N-(2-aminoethyl)-2-phenylacetamide

: 14435-46-2
2-<(2-phenoxyethoxy)methyl>oxirane

: 121508-95-0
N-{2-[2-Hydroxy-3-(2-phenoxy-ethoxy)-propylamino]-ethyl}-2-phenyl-acetamide

Guidance literature:: In isopropyl alcohol; for 16h; Heating;
DOI:10.1016/0223-5234(88)90138-9

Reference yield:

: 122-99-6,56257-90-0,9004-78-8
2-Phenoxyethanol

: 121508-95-0
N-{2-[2-Hydroxy-3-(2-phenoxy-ethoxy)-propylamino]-ethyl}-2-phenyl-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / NaH / tetrahydrofuran / 2 h / Heating

2: 44 percent / propan-2-ol / 16 h / Heating

With sodium hydride; In tetrahydrofuran; isopropyl alcohol;
DOI:10.1016/0223-5234(88)90138-9