Isoquinolin-8-yl-8-boronic acid

98%

Reagent Code: #199525
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CAS Number 721401-43-0

science Other reagents with same CAS 721401-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.98 g/mol
Formula C₉H₈BNO₂
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MDL Number MFCD11044913
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis and pharmaceutical research, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable for developing nitrogen-containing heterocyclic systems found in bioactive molecules. Commonly applied in the synthesis of potential therapeutic agents, including those targeting neurological disorders and cancer. Also serves as a building block in materials science for designing fluorescent probes and organic electronic materials due to the rigid isoquinoline scaffold.

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inventory 1g
10-20 days ฿3,120.00

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Isoquinolin-8-yl-8-boronic acid
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Used in organic synthesis and pharmaceutical research, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable for developing nitrogen-containing heterocyclic systems found in bioactive molecules. Commonly applied in the synthesis of potential therapeutic agents, including those targeting neurological disorders and cancer. Also serves as a building block in materials science for design

Used in organic synthesis and pharmaceutical research, particularly in Suzuki-Miyaura cross-coupling reactions to construct biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable for developing nitrogen-containing heterocyclic systems found in bioactive molecules. Commonly applied in the synthesis of potential therapeutic agents, including those targeting neurological disorders and cancer. Also serves as a building block in materials science for designing fluorescent probes and organic electronic materials due to the rigid isoquinoline scaffold.

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