(2-((Diethylamino)methyl)-4-fluorophenyl)boronic acid

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Reagent Code: #89606
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CAS Number 1704063-86-4

science Other reagents with same CAS 1704063-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.07 g/mol
Formula C₁₁H₁₇BFNO₂
badge Registry Numbers
MDL Number MFCD28384230
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. It serves as a key building block for the creation of complex organic molecules, especially those containing fluorophenyl groups. Its boronic acid moiety enables efficient coupling with aryl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds application in material science for synthesizing advanced polymers and organic electronic materials. The presence of the diethylamino group enhances its solubility and reactivity in various organic solvents, facilitating its use in diverse chemical transformations.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿19,380.00
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(2-((Diethylamino)methyl)-4-fluorophenyl)boronic 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 building block for the creation of complex organic molecules, especially those containing fluorophenyl groups. Its boronic acid moiety enables efficient coupling with aryl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds application in material science for synthesizing advanced polymers and organic electronic mat

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key building block for the creation of complex organic molecules, especially those containing fluorophenyl groups. Its boronic acid moiety enables efficient coupling with aryl halides, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it finds application in material science for synthesizing advanced polymers and organic electronic materials. The presence of the diethylamino group enhances its solubility and reactivity in various organic solvents, facilitating its use in diverse chemical transformations.

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