(4-(Benzyloxy)-3-(trifluoromethyl)phenyl)boronic acid

95%

Reagent Code: #90734
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CAS Number 1245014-05-4

science Other reagents with same CAS 1245014-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.05 g/mol
Formula C₁₄H₁₂BF₃O₃
badge Registry Numbers
MDL Number MFCD18383520
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling efficient coupling with aryl halides or other electrophiles. Additionally, it is employed in the development of bioactive molecules and complex organic frameworks, where its trifluoromethyl and benzyloxy substituents contribute to enhanced reactivity and stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,230.00
inventory 1g
10-20 days ฿2,950.00

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(4-(Benzyloxy)-3-(trifluoromethyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling efficient coupling with aryl halides or other electrophiles. Additionally, it is employed in the development of bioactive molecules and complex organic frameworks, where i

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. These reactions are essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key functional group, enabling efficient coupling with aryl halides or other electrophiles. Additionally, it is employed in the development of bioactive molecules and complex organic frameworks, where its trifluoromethyl and benzyloxy substituents contribute to enhanced reactivity and stability.

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