Urea, tris(phenylmethyl)-

Base Information

• Chemical Name: Urea, tris(phenylmethyl)-
• CAS No.: 19617-46-0
• Molecular Formula: C22H22N2O
• Molecular Weight: 330.429
• European Community (EC) Number: 664-900-0
• DSSTox Substance ID: DTXSID00402964
• Nikkaji Number: J1.683.015A
• Wikidata: Q82206492
• Mol file: 19617-46-0.mol

Synonyms:Urea, tris(phenylmethyl)-;N,N,N'-tribenzylurea;19617-46-0;DTXSID00402964;AKOS024336057

Chemical Property of Urea, tris(phenylmethyl)-

Chemical Property:

• XLogP3: 4
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 330.173213330
• Heavy Atom Count: 25
• Complexity: 360

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=C1)CNC(=O)N(CC2=CC=CC=C2)CC3=CC=CC=C3

Technology Process of Urea, tris(phenylmethyl)-

There total 5 articles about Urea, tris(phenylmethyl)- 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: 66.0%

dibenzylamine (103-49-1) + N,N'-dibenzyldiazenedicarboxamide → N,N,N'-tribenzylurea (19617-46-0)

Guidance literature:

With lithium 4-nitrophenolate; copper(ll) bromide; In tetrahydrofuran; at 50 ℃; for 0.333333h;

DOI:10.1246/bcsj.75.329

Reference yield:

dibenzylcarbamyl chloride (25370-09-6) → dibenzynitramine (95835-70-4) + dibenzylnitrosamine (5336-53-8) + N,N,N'-tribenzylurea (19617-46-0) + dibenzylammonium nitrate (20002-24-8) + benzaldehyde (100-52-7)

Guidance literature:

With silver nitrate; In acetonitrile; Product distribution; Ambient temperature; with moisture containing or well dried AgNO₃;

Reference yield:

dibenzylamine (103-49-1) → N,N,N'-tribenzylurea (19617-46-0)

Guidance literature:

Multi-step reaction with 2 steps

1: toluene; benzene

With toluene; benzene;

upstream raw materials:

dibenzylcarbamyl chloride

benzylamine

dibenzylamine

Refernces

• 1、 Nakajima, Masayuki,Anselme, Jean-Pierre. "THE REACTION OF N,N-DIBENZYLCARBAMOYL CHLORIDE WITH SILVER NITRATE". . p. 1105 - 1106. Retrieved 2007/10/02.