N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide

Base Information

Chemical Name:N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide
CAS No.:122892-38-0
Molecular Formula:C₁₈H₂₁FN₂O₂
Molecular Weight:316.375
Hs Code.:
DSSTox Substance ID:DTXSID90568841
Nikkaji Number:J459.979I
Wikidata:Q82455231

Synonyms:122892-38-0;SCHEMBL9815648;DTXSID90568841;N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide

Suppliers and Price of N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:316.15870608
Heavy Atom Count:23
Complexity:349

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C)CCOC1=CC=C(C=C1)CNC(=O)C2=CC=C(C=C2)F

Technology Process of N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide

There total 2 articles about N-({4-[2-(Dimethylamino)ethoxy]phenyl}methyl)-4-fluorobenzamide 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:

: 456-22-4
4-Fluorobenzoic acid

: 122892-38-0
N-[4-(2-Dimethylamino-ethoxy)-benzyl]-4-fluoro-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 0.5 h / Heating

2: Et₃N / CHCl₃ / 2 h / Ambient temperature

With thionyl chloride; triethylamine; In chloroform;
DOI:10.1248/cpb.40.202