(3-(Piperidin-1-ylsulfonyl)phenyl)boronic acid

95%

Reagent Code: #226428
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CAS Number 690662-96-5

science Other reagents with same CAS 690662-96-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.13 g/mol
Formula C₁₁H₁₆BNO₄S
badge Registry Numbers
MDL Number MFCD07783850
thermostat Physical Properties
Melting Point 166-168 ℃
Boiling Point 494.5±55.0 °C
inventory_2 Storage & Handling
Density 1.37±0.1 g/cm3
Storage 2-8°C, dry

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, while the piperidinylsulfonyl moiety can influence solubility and binding properties, making it valuable in the design of bioactive molecules and medicinal chemistry intermediates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,400.00
250mg
10-20 days ฿4,050.00
1g
10-20 days ฿10,880.00
(3-(Piperidin-1-ylsulfonyl)phenyl)boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, while the piperidinylsulfonyl moiety can influence solubility and binding properties, making it valuable in the design of bioactive molecules and medicinal chemistry intermediates.

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid group facilitates coupling with aryl halides, while the piperidinylsulfonyl moiety can influence solubility and binding properties, making it valuable in the design of bioactive molecules and medicinal chemistry intermediates.

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