3-Amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol

Base Information

Chemical Name:3-Amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol
CAS No.:54567-12-3
Molecular Formula:C₁₅H₁₃Cl₂N₃O
Molecular Weight:322.194
Hs Code.:
European Community (EC) Number:611-168-5
DSSTox Substance ID:DTXSID501151073

Synonyms:54567-12-3;DTXSID501151073;3-Amino-6-chloro-4-(2-chlorophenyl)-3,4-hydroxy-2-methylquinazoline;3-amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol;3-Amino-6-chloro-4-(2-chlorophenyl)-3,4-dihydro-2-methyl-4-quinazolinol

Suppliers and Price of 3-Amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol

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 2 raw suppliers

Chemical Property of 3-Amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol

Chemical Property:

Vapor Pressure:0mmHg at 25°C
XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:321.0435674
Heavy Atom Count:21
Complexity:433

Purity/Quality:: 99.9% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=NC2=C(C=C(C=C2)Cl)C(N1N)(C3=CC=CC=C3Cl)O
Uses 3-Amino-6-chloro-4-(2-chlorophenyl)-3,4-hydroxy-2-methylquinazoline is a useful intermediate in the preparation of triazolylbenzophenones useful as muscle relaxants, anticonvulsants, soporifics, and tranquilizers.

Technology Process of 3-Amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol

There total 1 articles about 3-Amino-6-chloro-4-(2-chlorophenyl)-2-methyl-3,4-dihydro-4-quinazolinol 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:

: 78-39-7
Triethyl orthoacetate

: 2958-36-3,53960-29-5
(2-amino-5-chloro-phenyl)-(2-chloro-phenyl)-methanone

: 54567-12-3
3-Amino-6-chloro-4-(2-chlorophenyl)-3,4-dihydro-4-hydroxy-2-methylquinazoline

Guidance literature:: With hydrazine hydrate; acetic acid; Yield given. Multistep reaction; 1)benzene, reflux 20 min ; 2)ethanol, room temp.17 h.;
DOI:10.1002/jhet.5570170331