3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid

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Reagent Code: #90205
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CAS Number 1228181-35-8

science Other reagents with same CAS 1228181-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.46 g/mol
Formula C₁₀H₁₂BClO₃
badge Registry Numbers
MDL Number MFCD18383681
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of biaryl compounds. Additionally, it finds application in the development of bioactive compounds, where the cyclopropylmethoxy group can influence the molecule's pharmacological properties. Its use is also seen in material science for creating advanced polymers and functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,971.00
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿9,000.00

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3-Chloro-4-(cyclopropylmethoxy)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of biaryl compounds. Additionally, it finds application in the development of bioactive compounds, where the cyclopropylmethoxy group can influence the molecule's p

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of biaryl compounds. Additionally, it finds application in the development of bioactive compounds, where the cyclopropylmethoxy group can influence the molecule's pharmacological properties. Its use is also seen in material science for creating advanced polymers and functional materials.

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