(5-Chloro-2,3-dimethoxypyridin-4-yl)boronic acid

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Reagent Code: #131574
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CAS Number 2096339-93-2

science Other reagents with same CAS 2096339-93-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.41 g/mol
Formula C₇H₉BClNO₄
badge Registry Numbers
MDL Number MFCD20231439
thermostat Physical Properties
Boiling Point 375.0±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.39±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Inert Gas

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecule assembly. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds found in drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its structural stability and reactivity profile.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,710.00
inventory 250mg
10-20 days ฿4,600.00
inventory 1g
10-20 days ฿11,970.00

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(5-Chloro-2,3-dimethoxypyridin-4-yl)boronic acid
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Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecule assembly. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds found in drug candidates targeting inflammatory diseases, cancer, and central nervous system

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors and other biologically active compounds. Its boronic acid functionality enables participation in Suzuki-Miyaura cross-coupling reactions, allowing for efficient formation of carbon-carbon bonds in complex molecule assembly. Commonly employed in medicinal chemistry for constructing pyridine-based scaffolds found in drug candidates targeting inflammatory diseases, cancer, and central nervous system disorders. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its structural stability and reactivity profile.

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