128676-84-6 Usage
Uses
Used in Organic Synthesis:
2-Chloroquinoline-3-boronic acid is used as a reagent in the field of organic synthesis, specifically for the Suzuki-Miyaura cross-coupling reaction. This reaction is a powerful method for the formation of carbon-carbon bonds, which is crucial for constructing complex organic molecules.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 2-Chloroquinoline-3-boronic acid is utilized as a building block for the creation of new drugs. Its ability to form stable bonds with a variety of organic molecules makes it a valuable component in the design and synthesis of potential therapeutic agents.
Used in Agrochemicals:
2-Chloroquinoline-3-boronic acid also finds application in the development of agrochemicals, where its chemical properties can be harnessed to create new compounds with pesticidal or herbicidal activity, contributing to more effective crop protection strategies.
Used in Research and Diagnostics:
Due to its fluorescent properties, 2-Chloroquinoline-3-boronic acid is used as a potentially valuable tool in research and diagnostics. Its fluorescence can be exploited for various analytical techniques, allowing for the detection and monitoring of biological processes or the development of new diagnostic assays.
Check Digit Verification of cas no
The CAS Registry Mumber 128676-84-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,6,7 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 128676-84:
(8*1)+(7*2)+(6*8)+(5*6)+(4*7)+(3*6)+(2*8)+(1*4)=166
166 % 10 = 6
So 128676-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H7BClNO2/c11-9-7(10(13)14)5-6-3-1-2-4-8(6)12-9/h1-5,13-14H
128676-84-6Relevant academic research and scientific papers
Method for preparing 2-chloroquinoline-3-boric acid
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Paragraph 0067-0069, (2021/06/23)
The invention belongs to the technical field of organic chemical synthesis, and particularly relates to a method for preparing 2-chloroquinoline-3-boric acid. The existing preparation method of 2-chloroquinoline-3-boric acid is relatively complex and wastes manpower and material resources. The invention provides the method for preparing 2-chloroquinoline-3-boric acid, which comprises the following steps: taking 2-chloroquinoline and a boron reagent as raw materials, carrying out 3-site substitution reaction on the 2-chloroquinoline under the action of alkali, and then hydrolyzing under the action of acid to obtain the 2-chloroquinoline-3-boric acid. The method has the advantages of mild reaction conditions, simple post-treatment purification, high yield and low cost.
