(3-(3-Hydroxypropyl)phenyl)boronic acid

98%

Reagent Code: #130379
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CAS Number 736989-98-3

science Other reagents with same CAS 736989-98-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.01 g/mol
Formula C₉H₁₃BO₃
badge Registry Numbers
MDL Number MFCD04115650
thermostat Physical Properties
Boiling Point 394.9±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

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, making it valuable in creating complex aromatic structures. Additionally, the boronic acid moiety can specifically bind to diols, serving as a starting material for developing sugar sensors or molecules with diol groups, suitable for targeted drug delivery systems or environmentally responsive materials. The hydroxypropyl side chain allows for further functionalization or improved solubility, useful in drug design and material science applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,980.00
inventory 1g
10-20 days ฿26,600.00

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(3-(3-Hydroxypropyl)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, making it valuable in creating complex aromatic structures. Additionally, the boronic acid moiety can specifically bind to diols, serving as a starting material for developing sugar sensors or molecules with diol groups, suitable for targeted drug delivery systems
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, making it valuable in creating complex aromatic structures. Additionally, the boronic acid moiety can specifically bind to diols, serving as a starting material for developing sugar sensors or molecules with diol groups, suitable for targeted drug delivery systems or environmentally responsive materials. The hydroxypropyl side chain allows for further functionalization or improved solubility, useful in drug design and material science applications.
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