(1H-Pyrrolo[3,2-b]pyridin-6-yl)boronic acid

95%

Reagent Code: #36182
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CAS Number 1253911-17-9

science Other reagents with same CAS 1253911-17-9

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Weight 161.9537 g/mol
Formula C₇H₇BN₂O₂
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MDL Number MFCD18255867
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(1H-Pyrrolo[3,2-b]pyridin-6-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The boronic acid group in the compound acts as a key functional group, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable for constructing heterocyclic compounds, which are often found in bioactive molecules and drugs. Additionally, it may be used in materials science for the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) or conductive polymers, due to its ability to form stable conjugated systems. Its application in medicinal chemistry also extends to the development of kinase inhibitors and other therapeutic agents targeting specific biological pathways.

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inventory 50mg
10-20 days ฿6,660.00

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(1H-Pyrrolo[3,2-b]pyridin-6-yl)boronic acid
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(1H-Pyrrolo[3,2-b]pyridin-6-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The boronic acid group in the compound acts as a key functional group, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable for construct

(1H-Pyrrolo[3,2-b]pyridin-6-yl)boronic acid is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create carbon-carbon bonds, enabling the synthesis of complex molecules, including drug candidates. The boronic acid group in the compound acts as a key functional group, facilitating the coupling with aryl or vinyl halides in the presence of a palladium catalyst. This makes it valuable for constructing heterocyclic compounds, which are often found in bioactive molecules and drugs. Additionally, it may be used in materials science for the development of organic electronic materials, such as organic light-emitting diodes (OLEDs) or conductive polymers, due to its ability to form stable conjugated systems. Its application in medicinal chemistry also extends to the development of kinase inhibitors and other therapeutic agents targeting specific biological pathways.

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