81216-93-5 Usage
Uses
Used in Synthetic Organic Chemistry:
2-(5-Bromo-2-thienyl)quinoline is used as a chemical intermediate for various synthetic organic chemistry applications due to its unique structure and reactivity. The presence of the thiophene ring and bromine atoms allows for a wide range of chemical reactions, making it a valuable compound in the synthesis of more complex molecules.
Used in Pharmaceutical Research:
2-(5-Bromo-2-thienyl)quinoline is used as a research compound in the development of new pharmaceuticals. Its unique structure and reactivity may contribute to the discovery of novel drug candidates, particularly in the areas of medicinal chemistry and drug design.
Used in Material Science:
2-(5-Bromo-2-thienyl)quinoline is used as a component in the development of new materials, such as organic semiconductors or advanced materials with specific properties. Its unique structure and reactivity can contribute to the creation of materials with improved performance characteristics.
Note: Due to the limited information available on the specific uses, health effects, or potential hazards of 2-(5-Bromo-2-thienyl)quinoline, it is important to exercise caution when handling 2-(5-BROMO-2-THIENYL)QUINOLINE and to follow proper safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 81216-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,1 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81216-93:
(7*8)+(6*1)+(5*2)+(4*1)+(3*6)+(2*9)+(1*3)=115
115 % 10 = 5
So 81216-93-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H8BrNS/c14-13-8-7-12(16-13)11-6-5-9-3-1-2-4-10(9)15-11/h1-8H
81216-93-5Relevant academic research and scientific papers
Smirnov, V. A.,Zimichev, A. V.,Lyzhova, G. A.,Lipkin, A. E.
, p. 28 - 31 (1982)
Depending on the substituent, the bromination of 4-(2-thienyl)thiazoles and 2-(2-thienyl)quinoline takes place in the 5 position of the thiophene or thiazole ring.When an amino group is present in the 2 position of the thiazole ring, bromination takes place in the 5 position of the thiazole ring.When excess brominating agent is present, a second bromine atom enters the 5 position of the free ring.
