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

Base Information

Chemical Name:Benzeneacetamide, N-[2-[[3-(2-hydroxy-3-phenylpr
CAS No.:121508-92-7
Molecular Formula:C₂₂H₃₀N₂O₃
Molecular Weight:370.492
Hs Code.:
DSSTox Substance ID:DTXSID30875400
Nikkaji Number:J1.562.153B

Synonyms:121508-92-7;BENZENEACETAMIDE, N-[2-[[3-(2-HYDROXY-3-PHENYLPR;DTXSID30875400

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

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-[[3-(2-hydroxy-3-phenylpr

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:13
Exact Mass:370.22564282
Heavy Atom Count:27
Complexity:380

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CCCOCC(CNCCNC(=O)CC2=CC=CC=C2)O

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

There total 2 articles about Benzeneacetamide, N-[2-[[3-(2-hydroxy-3-phenylpr 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: 47.0%

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

: 80910-19-6
2-<(3-phenylpropoxy)methyl>oxirane

: 121508-92-7
N-{2-[2-Hydroxy-3-(3-phenyl-propoxy)-propylamino]-ethyl}-2-phenyl-acetamide

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

Reference yield:

: 122-97-4
3-Phenyl-1-propanol

: 121508-92-7
N-{2-[2-Hydroxy-3-(3-phenyl-propoxy)-propylamino]-ethyl}-2-phenyl-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / NaH / tetrahydrofuran / 2 h / Heating

2: 47 percent / propan-2-ol / 16 h / Heating

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