(2-Chloro-6-fluoropyridin-3-yl)boronic acid

98%

Reagent Code: #130027
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CAS Number 1541206-12-5

science Other reagents with same CAS 1541206-12-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.35 g/mol
Formula C₅H₄BClFNO₂
badge Registry Numbers
MDL Number MFCD18257931
thermostat Physical Properties
Boiling Point 343.4±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.51±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and biologically active compounds. Its structure allows for cross-coupling reactions, especially Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in complex molecules. Commonly employed in the creation of herbicides and insecticides due to the presence of the chloro-fluoropyridine moiety, which enhances binding affinity and metabolic stability. Also utilized in medicinal chemistry for constructing novel drug candidates targeting central nervous system disorders and inflammatory diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,970.00
inventory 250mg
10-20 days ฿30,590.00

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(2-Chloro-6-fluoropyridin-3-yl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and biologically active compounds. Its structure allows for cross-coupling reactions, especially Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in complex molecules. Commonly employed in the creation of herbicides and insecticides due to the presence of the chloro-fluoropyridine moiety, which enhances binding affinity and metabolic stability. Also utilized in medicinal

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and biologically active compounds. Its structure allows for cross-coupling reactions, especially Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in complex molecules. Commonly employed in the creation of herbicides and insecticides due to the presence of the chloro-fluoropyridine moiety, which enhances binding affinity and metabolic stability. Also utilized in medicinal chemistry for constructing novel drug candidates targeting central nervous system disorders and inflammatory diseases.

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