N,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine

Base Information

Chemical Name:N,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine
CAS No.:97203-77-5
Molecular Formula:C19H20N4
Molecular Weight:304.395
Hs Code.:
DSSTox Substance ID:DTXSID90540460
Wikidata:Q82416483

Synonyms:97203-77-5;N,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine;DTXSID90540460;5-(N,N-Diethylamino)-4,6-diphenyl-1,2,3-triazine

Suppliers and Price of N,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine

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,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:304.16879665
Heavy Atom Count:23
Complexity:306

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)C1=C(N=NN=C1C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of N,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine

There total 2 articles about N,N-Diethyl-4,6-diphenyl-1,2,3-triazin-5-amine 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: 89.0%

: C₁₉H₂₀N⁽¹⁺⁾*FO₃S^(1-)

: 97203-77-5
(4,6-Diphenyl-[1,2,3]triazin-5-yl)-diethyl-amine

Guidance literature:: With sodium azide; In dichloromethane; for 16h; Ambient temperature;
DOI:10.1246/bcsj.58.1073

Reference yield:

: 886-38-4
diphenylcyclopropenone

: 97203-77-5
(4,6-Diphenyl-[1,2,3]triazin-5-yl)-diethyl-amine

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) ethyl fluorosulfate / 1.) CH₂Cl₂, room temp., 1h., 2.) 30 min

2: 89 percent / NaN₃ / CH₂Cl₂ / 16 h / Ambient temperature

With sodium azide; ethyl fluorosulfonate; In dichloromethane;
DOI:10.1246/bcsj.58.1073