2-Cyanophenylboronic acid, neopentyl ester

97%

Reagent Code: #89879
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CAS Number 214360-47-1

science Other reagents with same CAS 214360-47-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.06 g/mol
Formula C₁₂H₁₄BNO₂
badge Registry Numbers
MDL Number MFCD04039011
thermostat Physical Properties
Boiling Point 368.1°C
inventory_2 Storage & Handling
Density 1.08g/mL
Storage room temperature, dry

description Product Description

Used primarily in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Its boronic ester group facilitates efficient coupling with aryl halides, enabling the formation of complex organic molecules. Additionally, it serves as a reagent in the development of sensors and probes for detecting biologically relevant molecules, leveraging its ability to interact with diols and other functional groups. The compound’s stability and reactivity make it valuable in medicinal chemistry for designing drug candidates and in material science for synthesizing advanced polymers.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿666.00
inventory 200mg
10-20 days ฿351.00

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2-Cyanophenylboronic acid, neopentyl ester
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Used primarily in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Its boronic ester group facilitates efficient coupling with aryl halides, enabling the formation of complex organic molecules. Additionally, it serves as a reagent in the development of sensors and probes for detecting biologically relevant molecules, leveraging its ability to interact with diols an

Used primarily in organic synthesis as a versatile building block, particularly in Suzuki-Miyaura cross-coupling reactions to create biaryl compounds, which are essential in pharmaceuticals and agrochemicals. Its boronic ester group facilitates efficient coupling with aryl halides, enabling the formation of complex organic molecules. Additionally, it serves as a reagent in the development of sensors and probes for detecting biologically relevant molecules, leveraging its ability to interact with diols and other functional groups. The compound’s stability and reactivity make it valuable in medicinal chemistry for designing drug candidates and in material science for synthesizing advanced polymers.

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