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4(3H)-Quinazolinone, 8-hydroxy-2-methyl-3-(2-methylphenyl)-, also known as 8-Hydroxy-2-methyl-3-(2-methylphenyl)quinazolin-4(3H)-one, is a chemical compound belonging to the quinazolinone class. It is characterized by a quinazolinone core structure, with a hydroxyl group at the 8th position, a methyl group at the 2nd position, and a 2-methylphenyl group at the 3rd position. 4(3H)-Quinazolinone, 8-hydroxy-2-methyl-3-(2-methylphenyl)- has a molecular formula of C15H13NO2 and a molecular weight of 237.27 g/mol. It is an organic compound with potential applications in pharmaceuticals and chemical research, particularly in the development of new drugs and as a synthetic intermediate.

5060-53-7

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5060-53-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5060-53-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,6 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5060-53:
(6*5)+(5*0)+(4*6)+(3*0)+(2*5)+(1*3)=67
67 % 10 = 7
So 5060-53-7 is a valid CAS Registry Number.

5060-53-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-hydroxy-2-methyl-3-(2-methylphenyl)quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 4(3h)-quinazolinone,8-hydroxy-2-methyl-3-(2-methylphenyl)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5060-53-7 SDS

5060-53-7Relevant academic research and scientific papers

Design and evaluation of new hybrid pharmacophore quinazolino-tetrazoles as anticonvulsant strategy

Malik, Sachin,Khan, Suroor A.

, p. 207 - 223 (2014/03/21)

The anticonvulsant study of 25 newly synthesized quinazolin-4(3H)-one substituted 1H and 2H-tetrazoles (6a-6d, 7a-7b, 8a-8i, 8a′-8i′) was executed. The study employing the maximal electroshock and subcutaneous pentylenetetrazole (scPTZ) screens, the 'gold standards' in the preliminary anticonvulsant breakthrough and the neurotoxicity study applying the rotorod test unveiled a triad of compounds 6c, 7b and 8i′ as the looms amongst the compendium of synthesized compounds. The quantification data of these compounds following oral administration in rats showcased 7b to endorse a remarkable position in the MES screen with a protective indice (PI) of >39.67 and 6c in the scPTZ delineating a PI > 3.10, respectively. All the potent compounds were destitute of toxicity.

Synthesis and anticonvulsant evaluation of some novel 4(3H)-quinazolinones

El-Azab, Adel S.,ElTahir, Kamal E.H.,Attia, Sabry M.

, p. 837 - 848 (2012/08/07)

A series of novel quinazoline derivatives, methaqualone analogs, were synthesized, evaluated for their anticonvulsant activity against electrically and chemically (pentylenetetrazole, picrotoxin, and strychnine) induced seizures and compared with the stan

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