Quinolin-6-yl-6-boronic acid

≥95%

Reagent Code: #91025
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CAS Number 376581-24-7

science Other reagents with same CAS 376581-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.98 g/mol
Formula C₉H₈BNO₂
badge Registry Numbers
MDL Number MFCD03093100
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Quinolin-6-ylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the creation of complex organic molecules with high precision. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its versatility and reactivity make it a crucial component in medicinal chemistry and material science research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,925.00
inventory 5g
10-20 days ฿7,362.00

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Quinolin-6-yl-6-boronic acid
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Quinolin-6-ylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the creation of complex organic molecules with high precision. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to intera

Quinolin-6-ylboronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the creation of complex organic molecules with high precision. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. Its versatility and reactivity make it a crucial component in medicinal chemistry and material science research.

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