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Dibenzylamine hydrochloride

Base Information Edit
  • Chemical Name:Dibenzylamine hydrochloride
  • CAS No.:20455-68-9
  • Molecular Formula:C14H15 N . Cl H
  • Molecular Weight:233.741
  • Hs Code.:2923900090
  • European Community (EC) Number:243-834-2
  • UNII:668U27NZZ8
  • DSSTox Substance ID:DTXSID10942629
  • Mol file:20455-68-9.mol
Dibenzylamine hydrochloride

Synonyms:dibenzylamine;dibenzylamine acetate;dibenzylamine hydrochloride;iminodibenzyl

Suppliers and Price of Dibenzylamine hydrochloride
Supply Marketing:Edit
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
  • American Custom Chemicals Corporation
  • DIBENZYLAMINE HYDROCHLORIDE 98.00%
  • 5MG
  • $ 501.37
Total 8 raw suppliers
Chemical Property of Dibenzylamine hydrochloride Edit
Chemical Property:
  • Vapor Pressure:0.00115mmHg at 25°C 
  • Melting Point:260-262°C 
  • Boiling Point:300°Cat760mmHg 
  • Flash Point:143.3°C 
  • PSA:12.03000 
  • Density:1.028g/cm3 
  • LogP:4.16930 
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:4
  • Exact Mass:233.0971272
  • Heavy Atom Count:16
  • Complexity:137
Purity/Quality:

98%Min *data from raw suppliers

DIBENZYLAMINE HYDROCHLORIDE 98.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
  • Statements: 36/37/38 
  • Safety Statements: 26-36/37/39 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)CNCC2=CC=CC=C2.Cl
Technology Process of Dibenzylamine hydrochloride

There total 21 articles about Dibenzylamine hydrochloride 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:
Guidance literature:
With chloroform; 10% Pd/C; hydrogen; In methanol; at 20 ℃; for 2h; under 760.051 Torr; chemoselective reaction;
DOI:10.1016/j.tet.2008.09.072
Guidance literature:
N-benzylbenzamide; With dodecacarbonyl-triangulo-triruthenium; 1,1,3,3-tetramethyldisilazane; In toluene; at 20 - 50 ℃; for 24.17h; Inert atmosphere;
With hydrogenchloride; In 1,4-dioxane; ethyl acetate; toluene; at 20 ℃; for 0.5h;
DOI:10.1002/adsc.201200835
Guidance literature:
With aluminum oxide; silica gel; potassium carbonate; sodium percarbonate; sodium salt of 2,4-dichloro-6-hydroxy-1,3,5-triazine; In chloroform; column chromatography;
DOI:10.1021/ol036319g
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