65513-45-3 Usage
Uses
Used in Pharmaceutical and Medicinal Chemistry:
5-Bromo-6-methylquinoline is used as a building block for the synthesis of pharmaceuticals and bioactive molecules due to its unique reactivity and the ability to form diverse chemical structures.
Used in Research:
5-BroMo-6-Methylquinoline is utilized in research for its potential to contribute to the development of new drugs and materials, given its unique properties and reactivity.
Used in Materials Science:
5-Bromo-6-methylquinoline holds promise for applications in materials science, where its unique properties can be leveraged to create new materials with specific characteristics.
Overall, 5-Bromo-6-methylquinoline is a versatile chemical with applications across various fields, including chemistry, pharmaceuticals, and materials science, making it a valuable component in the development of innovative products and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 65513-45-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,1 and 3 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65513-45:
(7*6)+(6*5)+(5*5)+(4*1)+(3*3)+(2*4)+(1*5)=123
123 % 10 = 3
So 65513-45-3 is a valid CAS Registry Number.
65513-45-3Relevant academic research and scientific papers
SUBSTITUTED QUINOLINES AND METHODS FOR TREATING CANCER
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Paragraph 0239-0241, (2018/05/24)
Substituted quinoline compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds to treat, prevent or ameliorate cancer are provided.
BROMINATION OF QUINOLINE DERIVATIVES WITH N-BROMOSUCCINIMIDE. ISOMERIC COMPOSITION OF THE BROMINATION PRODUCTS BY PMR AND GLC
Tochilkin, A. I.,Kovel'man, I. R.,Prokof'ev, E. P.,Gracheva, I. N.,Levinskii, M. V.
, p. 892 - 897 (2007/10/02)
The bromination of quinoline and substituted quinolines with N-bromosuccinimide in concentrated H2SO4 takes place exclusively in the homocyclic part.Bromo-substituted quinolines can be obtained by this method.The bromination products were identified by PMR spectroscopy.The differences among the mono-, di-, and trisubstituted (in the benzene ring) compounds were established on the basis of the type of spectrum of the protons of the homocyclic part of the molecule.The compositions of the reaction mixtures were studied by GLC.
