Date published: 2025-9-25

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7-Chloroquinoline-4-boronic acid pinacol ester (CAS 871125-83-6)

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Alternate Names:
7-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
CAS Number:
871125-83-6
Molecular Weight:
289.56
Molecular Formula:
C15H17BClNO2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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7-Chloroquinoline-4-boronic acid pinacol ester has recently garnered attention for its potential applications in diverse scientific endeavors. This chemical compound is classified as a boron-containing heterocyclic compound, resulting from the reaction between a quinoline and a boronic acid. In scientific applications, 7-Chloroquinoline-4-boronic acid pinacol ester has been investigated for its catalytic potential in organic synthesis and its role as a reagent in synthesizing a diverse range of compounds like polymers and dyes. Additionally, it has demonstrated its utility in the synthesis of other compounds such as boronic acids, esters, and amines. Although the precise mechanism of action of 7-Chloroquinoline-4-boronic acid pinacol ester is not entirely comprehended, it is believed to function as a Lewis acid. As such, it is capable of forming bonds with Lewis bases, such as amines or alcohols.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

7-Chloroquinoline-4-boronic acid pinacol ester, 1 g

sc-233675
1 g
$129.00