4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride

Base Information

Chemical Name:4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride
CAS No.:132764-64-8
Molecular Formula:C20H24ClN5O2
Molecular Weight:401.8899
Hs Code.:
DSSTox Substance ID:DTXSID50157750

Synonyms:4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride;6,7-Dimethoxy-2-(4-phenyl-1-piperazinyl)-4-quinazolinamine monohydrochloride;132764-64-8;4-Quinazlolainamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride;DTXSID50157750;LS-139925

Suppliers and Price of 4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride

Chemical Property:

Vapor Pressure:1.55E-14mmHg at 25°C
Boiling Point:603.9°C at 760 mmHg
Flash Point:319°C
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:401.1618527
Heavy Atom Count:28
Complexity:467

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C(C=C2C(=C1)C(=NC(=N2)N3CCN(CC3)C4=CC=CC=C4)N)OC.Cl

Technology Process of 4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride

There total 1 articles about 4-Quinazolinamine, 6,7-dimethoxy-2-(4-phenyl-1-piperazinyl)-, monohydrochloride 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: 30.0%