5-Bromo-3-chloropyridazine

98%

Reagent Code: #151036
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CAS Number 1196155-33-5

science Other reagents with same CAS 1196155-33-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.43 g/mol
Formula C₄H₂BrClN₂
badge Registry Numbers
MDL Number MFCD13190293
thermostat Physical Properties
Boiling Point 303.7±22.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.859±0.06 g/cm3(Predicted)
Storage -20°C, Inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in research settings to introduce pyridazine rings into target compounds, enhancing biological activity in crop protection agents and medicinal chemistry.

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Test Parameter Specification
Appearance Off-White Powder
Purity 97.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,350.00
inventory 1g
10-20 days ฿4,000.00
inventory 5g
10-20 days ฿16,000.00

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5-Bromo-3-chloropyridazine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in research settings to introduce pyridazine rings into target compounds, enhancing biological activity in crop protection agents and medicinal chemistry.

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and plant growth regulators. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in research settings to introduce pyridazine rings into target compounds, enhancing biological activity in crop protection agents and medicinal chemistry.

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