2-(2-chlorophenyl)quinazoline-4(3H)-thione

Base Information

Chemical Name:2-(2-chlorophenyl)quinazoline-4(3H)-thione
CAS No.:18590-76-6
Molecular Formula:C14H9 Cl N2 S
Molecular Weight:0
Hs Code.:2933990090
DSSTox Substance ID:DTXSID90407281
Wikidata:Q82212530
Mol file:18590-76-6.mol

Synonyms:2-(2-chlorophenyl)quinazoline-4(3H)-thione;18590-76-6;2-(2-chlorophenyl)-1H-quinazoline-4-thione;2-(2-chlorophenyl)quinazoline-4-thiol;2-(2-chlorophenyl)-3,4-dihydroquinazoline-4-thione;DTXSID90407281;AKOS000116800;CS-0355949;EN300-08783;Z62436842

Suppliers and Price of 2-(2-chlorophenyl)quinazoline-4(3H)-thione

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

American Custom Chemicals Corporation
2-(2-CHLOROPHENYL)QUINAZOLINE-4(3H)-THIONE 95.00%
5G
$ 1759.28

American Custom Chemicals Corporation
2-(2-CHLOROPHENYL)QUINAZOLINE-4(3H)-THIONE 95.00%
2.5G
$ 1363.65

American Custom Chemicals Corporation
2-(2-CHLOROPHENYL)QUINAZOLINE-4(3H)-THIONE 95.00%
1G
$ 925.31

Total 5 raw suppliers

Chemical Property of 2-(2-chlorophenyl)quinazoline-4(3H)-thione

Chemical Property:

Vapor Pressure:9.56E-08mmHg at 25°C
Boiling Point:434.3°Cat760mmHg
Flash Point:216.5°C
PSA：60.77000
Density:1.36g/cm³
LogP:4.61280
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:272.0174972
Heavy Atom Count:18
Complexity:369

Purity/Quality:

97% ^*data from raw suppliers

2-(2-CHLOROPHENYL)QUINAZOLINE-4(3H)-THIONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C(=S)N=C(N2)C3=CC=CC=C3Cl

Technology Process of 2-(2-chlorophenyl)quinazoline-4(3H)-thione

There total 8 articles about 2-(2-chlorophenyl)quinazoline-4(3H)-thione 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: 65.1%

: 4765-50-8
2-(2-chlorophenyl)quinazolin-4(3H)-one

: 18590-76-6
2-(2-chlorophenyl)-4(3H)-quinazolinethione

Guidance literature:: With Lawessons reagent; In 1,4-dioxane; Reflux;
DOI:10.3109/14756366.2015.1018243

Reference yield: 57.0%

: 69949-33-3
2-(2-chlorophenyl)-4H-3,1-benzothiazine-4-thione

: 18590-76-6
2-(2-chlorophenyl)-4(3H)-quinazolinethione

Guidance literature:: With formamide; at 150 ℃; for 4h;
DOI:10.1002/hc.10148 DOI:10.1080/10426500390221078

Reference yield:

: 28144-70-9,88-68-6
anthranilic acid amide

: 18590-76-6
2-(2-chlorophenyl)-4(3H)-quinazolinethione

Guidance literature:: Multi-step reaction with 3 steps

1: dichloromethane / Reflux

2: potassium permanganate / N,N-dimethyl-formamide / Reflux

3: Lawessons reagent / toluene / Reflux

With Lawessons reagent; potassium permanganate; In dichloromethane; N,N-dimethyl-formamide; toluene;
DOI:10.1002/ardp.201200376