2-Benzyl-4-quinazolinethiol

Base Information

Chemical Name:2-Benzyl-4-quinazolinethiol
CAS No.:85690-42-2
Molecular Formula:C15H12N2S
Molecular Weight:252.33400
Hs Code.:
DSSTox Substance ID:DTXSID301333667
ChEMBL ID:CHEMBL1353467

Synonyms:2-benzyl-4-quinazolinethiol;2-benzyl-1H-quinazoline-4-thione;2-benzylquinazoline-4-thiol;85690-42-2;MLS001166410;SMR000549484;cid_806173;CHEMBL1353467;REGID_for_CID_806173;SCHEMBL10144731;BDBM54989;DTXSID301333667;HMS2885H13;AKOS000291540;AKOS000663472;11F-321S;2-(phenylmethyl)-1H-quinazoline-4-thione

Suppliers and Price of 2-Benzyl-4-quinazolinethiol

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-BENZYL-4-QUINAZOLINETHIOL 95.00%
5MG
$ 687.35

American Custom Chemicals Corporation
2-BENZYL-4-QUINAZOLINETHIOL 95.00%
10MG
$ 679.14

American Custom Chemicals Corporation
2-BENZYL-4-QUINAZOLINETHIOL 95.00%
1MG
$ 647.61

Total 0 raw suppliers

Chemical Property of 2-Benzyl-4-quinazolinethiol

Chemical Property:

PSA：60.77000
LogP:3.88320
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:252.07211956
Heavy Atom Count:18
Complexity:344

Purity/Quality:: 2-BENZYL-4-QUINAZOLINETHIOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC2=NC(=S)C3=CC=CC=C3N2

Technology Process of 2-Benzyl-4-quinazolinethiol

There total 4 articles about 2-Benzyl-4-quinazolinethiol 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: 64.0%

: 4765-56-4
glycosminine

: 85690-42-2
2-benzyl-4(3H)-quinazolinethione

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

Reference yield: 59.0%

: 84374-72-1
2-benzyl-4H-3,1-benzothiazine-4-thione

: 85690-42-2
2-benzyl-4(3H)-quinazolinethione

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

Reference yield:

: 58980-13-5
2-benzyl-4H-3,1-benzoxazine-4-one

: 85690-42-2
2-benzyl-4(3H)-quinazolinethione

Guidance literature:: Multi-step reaction with 2 steps

1: 30 percent / P₂S₅

2: 59 percent / formamide / 4 h / 150 °C

With tetraphosphorus decasulfide; formamide;
DOI:10.1080/10426500390221078