2-Benzylquinazolin-4(1H)-one

Base Information

Chemical Name:2-Benzylquinazolin-4(1H)-one
CAS No.:4765-56-4
Molecular Formula:C15H12N2O
Molecular Weight:236.273
Hs Code.:2933990090
Mol file:4765-56-4.mol

Synonyms:Glycosimine;Glycosminine;2-benzyl-3,4-dihydro-4-quinazolone;

Suppliers and Price of 2-Benzylquinazolin-4(1H)-one

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

Crysdot
2-Benzylquinazolin-4(1H)-one 95+%
1g
$ 653.00

Chemenu
2-benzylquinazolin-4(1H)-one 95%
1g
$ 617.00

American Custom Chemicals Corporation
2-BENZYL-4(3H)-QUINAZOLINONE 95.00%
5MG
$ 633.99

American Custom Chemicals Corporation
2-BENZYL-4(3H)-QUINAZOLINONE 95.00%
10MG
$ 631.85

American Custom Chemicals Corporation
2-BENZYL-4(3H)-QUINAZOLINONE 95.00%
1MG
$ 597.89

Alichem
2-Benzylquinazolin-4(1H)-one
1g
$ 563.41

Total 5 raw suppliers

Chemical Property of 2-Benzylquinazolin-4(1H)-one

Chemical Property:

Vapor Pressure:2.34E-07mmHg at 25°C
Boiling Point:422.9°C at 760 mmHg
Flash Point:209.5°C
PSA：46.01000
Density:1.21g/cm³
LogP:2.92620

Purity/Quality:

97% ^*data from raw suppliers

2-Benzylquinazolin-4(1H)-one 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

General Description 2-Benzylquinazolin-4(1H)-one is a quinazolinone derivative that has been studied for its urease inhibitory activity. While the abstract does not explicitly discuss this specific compound, related derivatives with benzyl substitutions at the 2-position of the quinazolinone scaffold have demonstrated potent inhibitory effects against Jack bean urease, suggesting that 2-Benzylquinazolin-4(1H)-one may also exhibit similar biological activity. The study highlights the significance of structural modifications in enhancing urease inhibition, particularly with substitutions on the quinazolinone core.

Technology Process of 2-Benzylquinazolin-4(1H)-one

There total 62 articles about 2-Benzylquinazolin-4(1H)-one 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: 97.0%

: 201230-82-2
carbon monoxide

: 1401675-18-0
C₂₁H₁₉IN₂O₂S

: 4765-56-4
glycosminine

Guidance literature:: With palladium diacetate; triethylamine; 1,4-di(diphenylphosphino)-butane; In tetrahydrofuran; at 100 ℃; for 12h; under 15201 Torr; Solvent; Pressure; Reagent/catalyst; Temperature; Autoclave;
DOI:10.1016/j.tetlet.2012.08.045

Reference yield: 95.0%

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

: 536-74-3
phenylacetylene

: 4765-56-4
glycosminine

Guidance literature:: With copper(l) iodide; 4-toluenesulfonyl azide; triethylamine; In acetonitrile; at 20 ℃; for 12h; Reagent/catalyst; Solvent; Time; Catalytic behavior; Inert atmosphere;
DOI:10.1016/j.tetlet.2017.06.026

Reference yield: 93.0%

: 140-29-4
phenylacetonitrile

: 118-92-3,159201-01-1,50816-84-7,80206-34-4,104809-47-4
anthranilic acid

: 4765-56-4
glycosminine

Guidance literature:: phenylacetonitrile; With hydroxylamine; at 120 ℃; for 1.5h;

anthranilic acid; at 150 ℃; for 2h;
DOI:10.1016/j.tetlet.2009.06.034