41320-96-1 Usage
Uses
Used in Pharmaceutical Industry:
3,4-Dibromoquinoline is used as an intermediate in the synthesis of various pharmaceutical compounds, contributing to the development of new drugs and therapies.
Used in Agrochemical Industry:
3,4-Dibromoquinoline is used as an intermediate in the synthesis of various agrochemical compounds, aiding in the development of pesticides and other agricultural chemicals.
Used in Antimalarial Applications:
3,4-Dibromoquinoline has been studied for its potential antimalarial properties, offering a possible alternative for the treatment of malaria.
Used in Anticancer Applications:
3,4-Dibromoquinoline has been studied for its potential anticancer properties, suggesting its use in the development of cancer treatments.
Used in Fluorescent Dyes Development:
3,4-Dibromoquinoline has been used in the development of fluorescent dyes, contributing to advancements in various scientific and industrial applications.
Used in Organic Light-Emitting Diodes (OLEDs) Development:
3,4-Dibromoquinoline has been used in the development of organic light-emitting diodes, playing a role in the advancement of display and lighting technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 41320-96-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,2 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41320-96:
(7*4)+(6*1)+(5*3)+(4*2)+(3*0)+(2*9)+(1*6)=81
81 % 10 = 1
So 41320-96-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H5Br2N/c10-7-5-12-8-4-2-1-3-6(8)9(7)11/h1-5H
41320-96-1Relevant academic research and scientific papers
Studies of one-pot double couplings on dibromoquinolines
Piala, Alexander,Mayi, Diyar,Handy, Scott T.
, p. 4147 - 4154 (2011/07/08)
In a series of studies, the regioselectivity of Suzuki couplings of dibromoquinolines has been investigated. In general, it is much harder to achieve high levels of regioselectivity in these systems compared to many of the other dibromoheteroaromatics that have been studied. Useful levels of selectivity could be achieved for both a 5,7-dibromoquinoline as well as 3,4-dibromoquinoline. Double Suzuki couplings could also be achieved on these two compounds.
Multiple regioselective functionalizations of quinolines via magnesiations
Boudet, Nadege,Lachs, Jennifer R.,Knochel, Paul
, p. 5525 - 5528 (2008/09/17)
A wide range of polyfunctionalized quinolines was prepared via chemo- and regioselective magnesiation reactions using appropriate Mg reagents, such as i-PrMgCl-LiCl, MesMgBr·LiCl, Mes2Mg·2LiBr, TMPMgCl·LiCl, and TMP2Mg·2LiCl. An application to the total synthesis of the biologically active compound talnetant was performed (six steps, 28%).
