61555-02-0 Usage
Chemical structure
Consists of a quinazolin-4(3H)-one ring with attached imidazole and methylphenyl groups.
Form
In the form of a hydrobromide salt.
Potential applications
May have pharmacological or medicinal applications.
Biological activities
Possesses a variety of biological activities, including anticancer, antimicrobial, and antiviral properties.
Improved properties
The hydrobromide salt form may offer improved solubility or stability for certain formulations or applications.
Check Digit Verification of cas no
The CAS Registry Mumber 61555-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,5 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61555-02:
(7*6)+(6*1)+(5*5)+(4*5)+(3*5)+(2*0)+(1*2)=110
110 % 10 = 0
So 61555-02-0 is a valid CAS Registry Number.
61555-02-0Relevant 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.
