2-PYRIDYLZINC BROMIDE

0.5MsolutioninTHF,MKSeal

Reagent Code: #226665
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CAS Number 218777-23-2

science Other reagents with same CAS 218777-23-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.39 g/mol
Formula C₅H₄BrNZn
badge Registry Numbers
MDL Number MFCD00671985
inventory_2 Storage & Handling
Density 0.974 g/cm3 at 25 °C
Storage 2-8°C, inert gas, flammable area, corrosive area, seal

description Product Description

Used as an organozinc reagent in cross-coupling reactions, particularly in Negishi coupling, to form carbon-carbon bonds between pyridyl groups and aryl or vinyl halides. Its main application is in the synthesis of complex organic molecules, especially in pharmaceuticals and agrochemicals, where the pyridine ring is a common structural motif. It offers good functional group tolerance and moderate reactivity, making it suitable for late-stage functionalization in multi-step syntheses. Often employed in air- and moisture-sensitive reactions, requiring inert handling techniques.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50ml
10-20 days ฿23,050.00
2-PYRIDYLZINC BROMIDE
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Used as an organozinc reagent in cross-coupling reactions, particularly in Negishi coupling, to form carbon-carbon bonds between pyridyl groups and aryl or vinyl halides. Its main application is in the synthesis of complex organic molecules, especially in pharmaceuticals and agrochemicals, where the pyridine ring is a common structural motif. It offers good functional group tolerance and moderate reactivity, making it suitable for late-stage functionalization in multi-step syntheses. Often employed in ai

Used as an organozinc reagent in cross-coupling reactions, particularly in Negishi coupling, to form carbon-carbon bonds between pyridyl groups and aryl or vinyl halides. Its main application is in the synthesis of complex organic molecules, especially in pharmaceuticals and agrochemicals, where the pyridine ring is a common structural motif. It offers good functional group tolerance and moderate reactivity, making it suitable for late-stage functionalization in multi-step syntheses. Often employed in air- and moisture-sensitive reactions, requiring inert handling techniques.

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