7471-65-0 Usage
Uses
Used in Pharmaceutical Industry:
1,2-DiMethylquinazolin-4(1H)-one is used as a key intermediate for the synthesis of various drugs, leveraging its unique quinazoline ring structure to contribute to the development of novel therapeutic agents.
Used in Medicinal Applications:
1,2-DiMethylquinazolin-4(1H)-one is used as an anticonvulsant and antidepressant agent, owing to its demonstrated properties in managing these conditions, thereby offering potential benefits to patients in need of such treatments.
Used in Cancer Research:
1,2-DiMethylquinazolin-4(1H)-one is used as a potential therapeutic agent in cancer treatment, as ongoing studies explore its efficacy in targeting and managing cancer cells, with the aim of improving patient outcomes.
Used in Corrosion Inhibition:
1,2-DiMethylquinazolin-4(1H)-one is used as a corrosion inhibitor, capitalizing on its chemical properties to protect materials from degradation, thereby extending their lifespan and reducing maintenance costs.
Used in Organic Chemistry:
1,2-DiMethylquinazolin-4(1H)-one is used as a precursor in the production of other organic compounds, highlighting its versatility and importance in the synthesis of a variety of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 7471-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 1 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7471-65:
(6*7)+(5*4)+(4*7)+(3*1)+(2*6)+(1*5)=110
110 % 10 = 0
So 7471-65-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O/c1-7-11-10(13)8-5-3-4-6-9(8)12(7)2/h3-6H,1-2H3
7471-65-0Relevant academic research and scientific papers
Synthesis of 4-Aminopyrimidines from 1,2,4-Oxadiazoles, I. A Novel General Method for the Preparation of 4-Aminoquinazolines and their Hetero Analogues
Korbonits, Dezsoe,Kiss, Pal,Simon, Kalman,Kolonits, Pal
, p. 3183 - 3193 (2007/10/02)
Catalytic hydrogenation of 3-(2-aminoaryl)-1,2,4-oxadiazoles (9, 12, 15, 18, 21) to 2-amino-N-acylarenecarboxamidines (10, 13, 16, 19, 22) followed by dehydration gave condensed 4-amino-pyrimidines (11, 14, 17, 20, 23), while the corresponding secondary amines (24) afforded 1,2-disubstituted 4-iminoquinazolines (26).Reduction and dehydration of 3--1,2,4-oxadiazoles (28) provided, via a somewhat different pathway, 4-(acylamino)quinazolines (31).
STUDIES ON 4-QUINAZOLINONES. PART IX. RANEY NICKEL DESULPHURISATION OF 4-THIOQUINAZOLINES: ALUMINA CATALYSED HYDRATION OF 1,4- AND 3,4-DIHYDROQUINAZOLINES
Chakrabarty, Manas,Chakravarty, Ajit K.,Pakrashi, Satyesh C.
, p. 445 - 450 (2007/10/02)
A number of 2-substituted 3,4-dihydroquinazolines and 1,2-disubstituted 1,4-dihydroquinazolines but not the 3-mono or 2,3-disubstituted derivatives, prepared by Raney nickel desulphurisation of the corresponding 4-thioquinazolines (IV), underwent unusual
