36023-06-0 Usage
General Description
8-Bromo-7-methoxyquinoline is a chemical compound with the molecular formula C10H8BrNO. It is a derivative of quinoline, and its structure consists of a quinoline ring with a bromine atom at the 8th position and a methoxy group at the 7th position. It is commonly used as a building block in the synthesis of various pharmaceuticals and agrochemicals. 8-Bromo-7-methoxyquinoline has been studied for its potential biological activities, including its antimicrobial, antitumor, and antioxidant properties. Additionally, 8-Bromo-7-methoxyquinoline has been investigated for its potential use in the development of fluorescent dyes and organic electronic materials.
Check Digit Verification of cas no
The CAS Registry Mumber 36023-06-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,0,2 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 36023-06:
(7*3)+(6*6)+(5*0)+(4*2)+(3*3)+(2*0)+(1*6)=80
80 % 10 = 0
So 36023-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H6BrNO/c10-8-7(12)4-3-6-2-1-5-11-9(6)8/h1-5,12H
36023-06-0Relevant articles and documents
NOVEL COMPOUND, PHOTOACID GENERATOR CONTAINING THE COMPOUND, AND PHOTOSENSITIVE RESIN COMPOSITION CONTAINING THE PHOTOACID GENERATOR
-
, (2018/12/05)
PROBLEM TO BE SOLVED: To provide a nonionic photoacid generator with high acid generation quantum yield. SOLUTION: The present invention provides a compound represented by formula (2) (where, ring Ar is a benzene ring, naphthalene ring, thiophene ring or
Kinetic Resolution of Axially Chiral 5- or 8-Substituted Quinolines via Asymmetric Transfer Hydrogenation
Wang, Jie,Chen, Mu-Wang,Ji, Yue,Hu, Shu-Bo,Zhou, Yong-Gui
supporting information, p. 10413 - 10416 (2016/09/04)
An efficient kinetic resolution of axially chiral 5- or 8-substituted quinoline derivatives was developed through asymmetric transfer hydrogenation of heteroaromatic moiety, simultaneously obtaining two kinds of axially chiral skeletons with up to 209 of selectivity factor. This represents the first successful application of asymmetric transfer hydrogenation of heteroaromatics in kinetic resolution of axially chiral biaryls.
