4-(2-Methoxyethylaminocarbonyl)phenylboronic acid

95%

Reagent Code: #209407
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CAS Number 850589-34-3

science Other reagents with same CAS 850589-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.0335 g/mol
Formula C₁₀H₁₄BNO₄
badge Registry Numbers
MDL Number MFCD04115682
thermostat Physical Properties
Melting Point 120-124 °C
inventory_2 Storage & Handling
Density 1.21 g/cm3
Storage 2-8°C, dry

description Product Description

Used in organic synthesis as a key intermediate 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 methoxyethylaminocarbonyl moiety enhances solubility and can act as a directing or stabilizing group. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and fluorescent probes for sensing applications. Also utilized in the development of glucose-responsive materials due to the affinity of boronic acids for diols, making it suitable for smart drug delivery systems and biosensors.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,020.00
1g
10-20 days ฿7,670.00
250mg
10-20 days ฿2,790.00
4-(2-Methoxyethylaminocarbonyl)phenylboronic acid
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Used in organic synthesis as a key intermediate 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 methoxyethylaminocarbonyl moiety enhances solubility and can act as a directing or stabilizing group. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and fluorescent probes for sensing applications. Also util

Used in organic synthesis as a key intermediate 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 methoxyethylaminocarbonyl moiety enhances solubility and can act as a directing or stabilizing group. Commonly employed in the preparation of bioactive molecules, including kinase inhibitors and fluorescent probes for sensing applications. Also utilized in the development of glucose-responsive materials due to the affinity of boronic acids for diols, making it suitable for smart drug delivery systems and biosensors.

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