6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline

Base Information

Chemical Name:6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline
CAS No.:84571-02-8
Molecular Formula:C19H17ClN2S
Molecular Weight:340.876
Hs Code.:
DSSTox Substance ID:DTXSID30574385

Synonyms:84571-02-8;6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline;DTXSID30574385

Suppliers and Price of 6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline

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 6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline

Chemical Property:

XLogP3:5.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:340.0800974
Heavy Atom Count:23
Complexity:401

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(S1)C2NC(C3=C(N2)C=CC(=C3)Cl)C4=CC=CC=C4

Technology Process of 6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline

There total 2 articles about 6-Chloro-2-(5-methylthiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydroquinazoline 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: 98.0%

: 13679-70-4
5-methylthiophene-2-carboxaldehyde

: 1824-70-0
2-amino-5-chlorobenzhydrylamine

: 84571-02-8
6-Chloro-2-(5-methyl-thiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydro-quinazoline

Guidance literature:: With acetic acid; In ethanol; for 3h; Heating;

Reference yield:

: 18097-52-4
2-amino-5-chlorobenzophenone oxime

: 84571-02-8
6-Chloro-2-(5-methyl-thiophen-2-yl)-4-phenyl-1,2,3,4-tetrahydro-quinazoline

Guidance literature:: Multi-step reaction with 2 steps

1: 94.6 percent / Zn, CH₃COONH₄ / aq. NH₃; ethanol / 3 h / Heating

2: 98 percent / glacial acetic acid / ethanol / 3 h / Heating

With ammonium acetate; acetic acid; zinc; In ammonium hydroxide; ethanol;