128676-84-6 Usage
General Description
2-Chloroquinoline-3-boronic acid is a heterocyclic compound containing a boronic acid functional group. It is a derivative of quinoline, a chemical compound with antimalarial and antibacterial properties. The boronic acid moiety in 2-Chloroquinoline-3-boronic acid makes it a useful reagent in organic synthesis, particularly in the field of Suzuki-Miyaura cross-coupling reaction. 2-CHLOROQUINOLINE-3-BORONIC ACID has also demonstrated potential usefulness in the development of pharmaceuticals and agrochemicals due to its ability to form stable bonds with a variety of organic molecules. Additionally, it has been investigated for its fluorescent properties, making it a potentially valuable tool in research and diagnostics.
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 articles and documents
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.
