(4-vinylphenyl)boronic acid pinacol ester

98%

Reagent Code: #245465
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CAS Number 870004-04-9

science Other reagents with same CAS 870004-04-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.1200 g/mol
Formula C₁₄H₁₉BO₂
badge Registry Numbers
MDL Number MFCD18733870
thermostat Physical Properties
Boiling Point 323.5±21.0℃(Predicted)
inventory_2 Storage & Handling
Density 0.98±0.1g/ml(Predicted)
Storage 2-8℃, dry, sealed

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated organic compounds, particularly in the development of organic electronic materials and liquid crystals. Serves as a key building block in polymer chemistry for creating functionalized polymers with tailored electronic properties. Also applied in the preparation of sensors and molecular recognition systems due to its boronate ester group, which can be selectively deprotected to form boronic acids for bioconjugation or sensing applications. Stable and easy to handle, making it suitable for multi-step syntheses in pharmaceutical and agrochemical research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,730.00
inventory 5g
10-20 days ฿6,490.00
inventory 25g
10-20 days ฿27,680.00

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(4-vinylphenyl)boronic acid pinacol ester
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Used in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated organic compounds, particularly in the development of organic electronic materials and liquid crystals. Serves as a key building block in polymer chemistry for creating functionalized polymers with tailored electronic properties. Also applied in the preparation of sensors and molecular recognition systems due to its boronate ester group, which can be selectively deprotected to form boronic acids for bioconjugation or sensing applica

Used in Suzuki-Miyaura cross-coupling reactions to synthesize conjugated organic compounds, particularly in the development of organic electronic materials and liquid crystals. Serves as a key building block in polymer chemistry for creating functionalized polymers with tailored electronic properties. Also applied in the preparation of sensors and molecular recognition systems due to its boronate ester group, which can be selectively deprotected to form boronic acids for bioconjugation or sensing applications. Stable and easy to handle, making it suitable for multi-step syntheses in pharmaceutical and agrochemical research.

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