(2,4-Difluoro-3-(hydroxymethyl)phenyl)boronic acid

95%

Reagent Code: #178095
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CAS Number 1352813-46-7

science Other reagents with same CAS 1352813-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.94 g/mol
Formula C₇H₇BF₂O₃
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MDL Number MFCD22570910
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings to design drug candidates targeting cancer, inflammation, and central nervous system disorders. The presence of fluorine atoms enhances metabolic stability and influences binding affinity, which is beneficial in optimizing drug potency and pharmacokinetics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,680.00
inventory 1g
10-20 days ฿6,450.00
inventory 5g
10-20 days ฿25,370.00

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(2,4-Difluoro-3-(hydroxymethyl)phenyl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings to design drug candidates targeting cancer, inflammation, and central nervous system disorders. The presence of fluorine at

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other biologically active molecules. Its boronic acid functional group enables participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in medicinal chemistry for constructing carbon-carbon bonds. Commonly employed in research settings to design drug candidates targeting cancer, inflammation, and central nervous system disorders. The presence of fluorine atoms enhances metabolic stability and influences binding affinity, which is beneficial in optimizing drug potency and pharmacokinetics.

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