5-Bromo-2,3-dichloropyridine

98%

Reagent Code: #144840
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CAS Number 97966-00-2

science Other reagents with same CAS 97966-00-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.89 g/mol
Formula C₅H₂BrCl₂N
badge Registry Numbers
MDL Number MFCD04112492
thermostat Physical Properties
Melting Point 35-37 °C
Boiling Point 234°C/760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its halogen substitution pattern that allows for selective chemical modifications. Its structure supports coupling reactions in the development of active ingredients targeting weed and pest control in crop protection. Also utilized in pharmaceutical research for building blocks in heterocyclic compounds, where the bromo and chloro groups enable sequential functionalization for drug discovery. Common in Suzuki and other palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds in complex molecule assembly.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿580.00
inventory 25g
10-20 days ฿2,330.00
inventory 100g
10-20 days ฿9,300.00

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5-Bromo-2,3-dichloropyridine
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its halogen substitution pattern that allows for selective chemical modifications. Its structure supports coupling reactions in the development of active ingredients targeting weed and pest control in crop protection. Also utilized in pharmaceutical research for building blocks in heterocyclic compounds, where the bromo and chloro groups enable sequential functionalization for drug discovery. Co

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its halogen substitution pattern that allows for selective chemical modifications. Its structure supports coupling reactions in the development of active ingredients targeting weed and pest control in crop protection. Also utilized in pharmaceutical research for building blocks in heterocyclic compounds, where the bromo and chloro groups enable sequential functionalization for drug discovery. Common in Suzuki and other palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds in complex molecule assembly.

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