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4(3H)-Quinazolinone, 2-(hydroxymethyl)-3-(2-methylphenyl)- is a complex organic compound with the molecular formula C12H11NO2. It is a derivative of quinazolinone, a heterocyclic compound with a quinazoline ring system. This specific compound features a hydroxymethyl group at the 2-position and a 2-methylphenyl group at the 3-position, which are both attached to the quinazolinone core. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and chemical compounds due to its unique structure and properties. The compound is also known for its potential applications in medicinal chemistry, particularly in the development of anticancer and antiviral agents.

5060-49-1

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5060-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5060-49-1 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, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5060-49:
(6*5)+(5*0)+(4*6)+(3*0)+(2*4)+(1*9)=71
71 % 10 = 1
So 5060-49-1 is a valid CAS Registry Number.

5060-49-1SDS

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 2-(hydroxymethyl)-3-(2-methylphenyl)quinazolin-4-one

1.2 Other means of identification

Product number -
Other names 2-hydroxymethyl-3-o-tolyl-3H-quinazolin-4-one

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:5060-49-1 SDS

5060-49-1Upstream product

5060-49-1Downstream Products

5060-49-1Relevant academic research and scientific papers

Synthesis and central nervous system activity of quinazolones related to 2 methyl 3 (o tolyl) 4 (3H) quinazolone (methaqualone)

Ager,Harrison,Kennewell,Taylor

, p. 379 - 386 (2007/10/08)

A number of derivatives of 2-methyl-3-(o-tolyl)-4(3H)-quinazolone bearing new substituents on the 2-methyl group have been synthesized. It was established that most substitutions at this position reduce or remove the CNS depressant activity of methaqualone. From the series prepared only the 2-fluoromethyl derivative or certain isothiouronium salts, which could be hydrolyzed in vivo to the 2-mercaptomethyl derivative, showed activity of the same magnitude as methaqualone.

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