(3-Chloro-5-isopropoxyphenyl)boronic acid

95%

Reagent Code: #131917
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CAS Number 1887126-63-7

science Other reagents with same CAS 1887126-63-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.45 g/mol
Formula C₉H₁₂BClO₃
badge Registry Numbers
MDL Number MFCD30716823
thermostat Physical Properties
Boiling Point 369.2±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.23±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The chloro and isopropoxy substituents provide sites for further functionalization or influence electronic and steric properties in target molecules. Commonly applied in the synthesis of bioactive intermediates and functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿3,120.00
1g
10-20 days ฿8,400.00
5g
10-20 days ฿31,840.00
(3-Chloro-5-isopropoxyphenyl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The chloro and isopropoxy substituents provide sites for further functionalization or influence electronic and steric properties in target molecules. Commonly applied in the synthesis of bioactive inte

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex aromatic compounds. The chloro and isopropoxy substituents provide sites for further functionalization or influence electronic and steric properties in target molecules. Commonly applied in the synthesis of bioactive intermediates and functional materials.

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