84839-95-2 Usage
Uses
Used in Pharmaceutical Industry:
8-Bromo-6-methylquinoline is used as a building block for the synthesis of pharmaceuticals due to its antimicrobial, anti-inflammatory, and analgesic properties. It plays a significant role in the development of new drugs, contributing to the creation of potentially valuable compounds for medical applications.
Used in Agrochemical Industry:
In the agrochemical sector, 8-Bromo-6-methylquinoline is utilized as a precursor in the production of agrochemicals. Its antimicrobial properties make it a valuable component in the development of pesticides and other agricultural chemicals to protect crops and enhance yield.
Used in Research and Development:
8-Bromo-6-methylquinoline is also employed as a research compound in the scientific community. Its unique structure and properties make it an important tool for studying the synthesis and pharmacological effects of various bioactive molecules, furthering the understanding of its potential applications in medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 84839-95-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,3 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 84839-95:
(7*8)+(6*4)+(5*8)+(4*3)+(3*9)+(2*9)+(1*5)=182
182 % 10 = 2
So 84839-95-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrN/c1-7-5-8-3-2-4-12-10(8)9(11)6-7/h2-6H,1H3
84839-95-2Relevant academic research and scientific papers
Catalytic dehydrogenative borylation of terminal alkynes by a SiNN pincer complex of iridium
Lee, Chun-I,Zhou, Jia,Ozerov, Oleg V.
, p. 3560 - 3566 (2013/04/23)
Compounds with carbon-boron bonds are versatile intermediates for building more complex molecules via the elaboration of the carbon-boron bonds into other carbon-element bonds. The synthesis of carbon-boron bonds by catalytic dehydrogenative borylation of carbon-hydrogen bonds with dialkoxyboranes (RO)2BH is particularly attractive. It has been demonstrated for a variety of carbon-hydrogen bond types but not for the C(sp)-H bonds of terminal alkynes, for which hydroboration of the triple bond is a competing process. We report a new iridium catalyst that is strictly chemoselective for C-H borylation of terminal alkynes. The key to the success of this catalyst appears to be the new ancillary SiNN pincer ligand that combines amido, quinoline, and silyl donors and gives rise to structurally unusual Ir complexes. A variety of terminal alkynes (RC≡C-H) can be converted to their alkynylboronates (RC≡C-Bpin, where pin = pinacolate) in high yield and purity within minutes at ambient temperature.
