61555-05-3 Usage
Pharmaceutical use
Commonly used in pharmaceutical research and development.
Biological activities
Has potential therapeutic applications due to its antimicrobial and anticancer properties.
Solubility and stability
The hydrobromide salt form of this compound allows for improved solubility and stability, making it easier to handle and use in experimental and clinical settings.
Pharmacokinetics and pharmacodynamics
The presence of the hydrobromide counterion can impact the pharmacokinetics and pharmacodynamics of the compound, influencing its bioavailability and distribution in the body.
Therapeutic value
Has potential therapeutic value and is of interest in the pharmaceutical industry for further study and development.
Check Digit Verification of cas no
The CAS Registry Mumber 61555-05-3 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 61555-05:
(7*6)+(6*1)+(5*5)+(4*5)+(3*5)+(2*0)+(1*5)=113
113 % 10 = 3
So 61555-05-3 is a valid CAS Registry Number.
61555-05-3Relevant articles and documents
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.
