(4-((pyridin-2-ylamino)methyl)phenyl)boronic acid

95%

Reagent Code: #36810
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CAS Number 568581-08-8

science Other reagents with same CAS 568581-08-8

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scatter_plot Molecular Information
Weight 228.05482 g/mol
Formula C₁₂H₁₃BN₂O₂
badge Registry Numbers
MDL Number MFCD31916456
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its pyridine moiety enhances stability and reactivity, allowing for efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of bioactive compounds and materials science, where its structural properties contribute to the design of novel polymers and catalysts. Its applications also extend to medicinal chemistry, where it is used in the creation of drug candidates targeting various diseases.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿53,298.00

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(4-((pyridin-2-ylamino)methyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its pyridine moiety enhances stability and reactivity, allowing for efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of bioactive compounds and

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a boronic acid reagent. It facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its pyridine moiety enhances stability and reactivity, allowing for efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of bioactive compounds and materials science, where its structural properties contribute to the design of novel polymers and catalysts. Its applications also extend to medicinal chemistry, where it is used in the creation of drug candidates targeting various diseases.

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