1210-03-3 Usage
Uses
Used in Pharmaceutical Industry:
3-methylbenzo[f]quinolin-1(4H)-one is used as a pharmaceutical candidate for its potential anticancer properties, as it may exhibit inhibitory effects on tumor growth and progression. Its unique structure and biological activities make it a promising compound for the development of new drugs targeting various types of cancer.
Used in Medicinal Chemistry Research:
3-methylbenzo[f]quinolin-1(4H)-one serves as a key compound in medicinal chemistry research, where it is studied for its potential anti-inflammatory and antimicrobial activities. Its heterocyclic structure and the presence of a methyl group at the 3-position contribute to its pharmacological properties, making it a valuable subject for further investigation and development of novel therapeutic agents.
Used in Drug Development:
3-methylbenzo[f]quinolin-1(4H)-one is utilized in drug development as a lead compound for the creation of new pharmaceuticals. Its potential biological activities and pharmacological properties, such as anticancer, anti-inflammatory, or antimicrobial effects, make it a valuable starting point for the design and synthesis of novel drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 1210-03-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,1 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1210-03:
(6*1)+(5*2)+(4*1)+(3*0)+(2*0)+(1*3)=23
23 % 10 = 3
So 1210-03-3 is a valid CAS Registry Number.
1210-03-3Relevant academic research and scientific papers
Spectral Studied of Some Substituted Arylthiobenzoquinolines
Bahuguna, R. P.,Joshi, Y. C.,Dobhal, M. P.,Pande, R. K.,Joshi, B. C.
, p. 957 - 960 (2007/10/02)
Synthesis and spectral studies (ir, 1H nmr, ms) of 1- and 3-substituted arylthiobenzoquinolines (IIIa-IIIc, IVa-IVc) obtained through nucleophilic displacement of the corresponding halobenzoquinoline by various thiols (a-c) were done.
