220506-64-9 Usage
Uses
Used in Pharmaceutical Research:
(2-CHLORO-8-METHOXY-3-QUINOLINYL)-BORONIC ACID is used as a building block for the synthesis of various biologically active compounds, contributing to the development of new drugs and therapies.
Used in Organic Synthesis:
(2-CHLORO-8-METHOXY-3-QUINOLINYL)-BORONIC ACID is used as a reagent in organic synthesis processes, facilitating the formation of stable complexes with other molecules and enhancing the efficiency of chemical reactions.
Used in Anticancer Applications:
(2-CHLORO-8-METHOXY-3-QUINOLINYL)-BORONIC ACID is used as an anti-cancer agent for its ability to inhibit enzymes involved in cancer cell proliferation, potentially leading to the development of new cancer treatments.
Used in Antimicrobial Applications:
(2-CHLORO-8-METHOXY-3-QUINOLINYL)-BORONIC ACID is used as an antimicrobial agent, leveraging its potential to combat microbial infections and contribute to the development of new antimicrobial drugs.
Used in Anti-inflammatory Applications:
(2-CHLORO-8-METHOXY-3-QUINOLINYL)-BORONIC ACID is used as an anti-inflammatory agent, potentially aiding in the treatment of inflammation-related conditions and contributing to the development of new anti-inflammatory medications.
Check Digit Verification of cas no
The CAS Registry Mumber 220506-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,5,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 220506-64:
(8*2)+(7*2)+(6*0)+(5*5)+(4*0)+(3*6)+(2*6)+(1*4)=89
89 % 10 = 9
So 220506-64-9 is a valid CAS Registry Number.
220506-64-9Relevant academic research and scientific papers
Preparation of new 3-hydroxyquinoline alkaloid, jineol and its ether derivatives using directed ortho-lithiation of chloroquinoline as the key step
Tagawa, Yoshinobu,Yamashita, Hiroyuki,Nomura, Manami,Goto, Yoshinobu
, p. 2379 - 2387 (2007/10/03)
A new alkaloid, jineol (3,8-dihydroxyquinoline) was conveniently prepared employing directed ortho-lithiation of chloroquinoline for 3-position of quinoline ring. Moreover, the ether derivatives of jineol were obtained by the reaction of jineol with alkyl
