5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine

Base Information

Chemical Name:5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine
CAS No.:32524-44-0
Molecular Formula:C14H13N7
Molecular Weight:279.34
Hs Code.:2933599090
Nikkaji Number:J35.419H
Mol file:32524-44-0.mol

Synonyms:BRN 0036560;5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine;32524-44-0;5-beta-Naphthyl-2:4:6-triaminoazopyrimidine;Pyrimidine, 5-(beta-naphthylazo)-2,4,6-triamino-;5-25-18-00286 (Beilstein Handbook Reference)

Suppliers and Price of 5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine

Supply Marketing:

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

Total 5 raw suppliers

5-β-NAPHTHYL-2:4:6-TRIAMINOAZO-PYRIMIDINE" href="//Mopai89.lookchem.com/products/CasNo-32524-44-0--span-xmlns-style-font-weight-bold-5--span-beta--NAPHTHYL-2-4-6-TRIAMINOAZO-PYRIMIDINE-30975484.html">
5-β-NAPHTHYL-2:4:6-TRIAMINOAZO-PYRIMIDINE" href="//antimex.lookchem.com/products/CasNo-32524-44-0--span-xmlns-style-font-weight-bold-5--span-beta--NAPHTHYL-2-4-6-TRIAMINOAZO-PYRIMIDINE-27208188.html">

Chemical Property of 5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine

Chemical Property:

Vapor Pressure:1.99E-17mmHg at 25°C
Refractive Index:1.8260 (estimate)
Boiling Point:662.6°C at 760 mmHg
PKA:5.30±0.10(Predicted)
Flash Point:354.5°C
PSA：130.02000
Density:1.53g/cm³
LogP:3.23320
XLogP3:2.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:2
Exact Mass:279.12324344
Heavy Atom Count:21
Complexity:362

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C=C(C=CC2=C1)N=NC3=C(N=C(N=C3N)N)N

Technology Process of 5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine

There total 1 articles about 5-(beta-Naphthylazo)-2,4,6-triaminopyrimidine 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: