(5-Chloro-6-methylpyridin-3-yl)boronic acid

97%

Reagent Code: #131102
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CAS Number 1334405-66-1

science Other reagents with same CAS 1334405-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 171.39 g/mol
Formula C₆H₇BClNO₂
badge Registry Numbers
MDL Number MFCD18255104
thermostat Physical Properties
Boiling Point 322.4±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34±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 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, which are prevalent in drugs targeting inflammation, cancer, and central nervous system disorders. Also utilized in agrochemical research for designing novel active ingredients with improved selectivity and stability.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,700.00
inventory 1g
10-20 days ฿28,000.00

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(5-Chloro-6-methylpyridin-3-yl)boronic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, 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, which are prevalent in drugs targeting inflammation, cancer, and central nervous sys

Used as a key intermediate in the synthesis of pharmaceuticals, 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, which are prevalent in drugs targeting inflammation, cancer, and central nervous system disorders. Also utilized in agrochemical research for designing novel active ingredients with improved selectivity and stability.

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