4-(Bromomethyl)-4'-methyl-2,2'-bipyridyl

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Reagent Code: #147465
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CAS Number 81998-05-2

science Other reagents with same CAS 81998-05-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.14 g/mol
Formula C₁₂H₁₁BrN₂
badge Registry Numbers
MDL Number MFCD08275265
thermostat Physical Properties
Melting Point 74.0-78.0°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a key intermediate in the synthesis of functionalized bipyridyl ligands for coordination chemistry. It enables the attachment of bipyridyl complexes to polymers, surfaces, or biomolecules through the reactive bromomethyl group. Commonly employed in the development of ruthenium- or iridium-based photoredox catalysts, where the methyl group can be further modified to tune electronic properties. Also applied in the preparation of metallo-supramolecular architectures, such as molecular cages and switches, due to its ability to form stable complexes with transition metals. Its reactivity allows for easy alkylation of nitrogen-containing heterocycles, facilitating the construction of complex multidentate ligands.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿7,500.00
inventory 1g
10-20 days ฿33,500.00

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4-(Bromomethyl)-4'-methyl-2,2'-bipyridyl
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Used primarily as a key intermediate in the synthesis of functionalized bipyridyl ligands for coordination chemistry. It enables the attachment of bipyridyl complexes to polymers, surfaces, or biomolecules through the reactive bromomethyl group. Commonly employed in the development of ruthenium- or iridium-based photoredox catalysts, where the methyl group can be further modified to tune electronic properties. Also applied in the preparation of metallo-supramolecular architectures, such as molecular cage

Used primarily as a key intermediate in the synthesis of functionalized bipyridyl ligands for coordination chemistry. It enables the attachment of bipyridyl complexes to polymers, surfaces, or biomolecules through the reactive bromomethyl group. Commonly employed in the development of ruthenium- or iridium-based photoredox catalysts, where the methyl group can be further modified to tune electronic properties. Also applied in the preparation of metallo-supramolecular architectures, such as molecular cages and switches, due to its ability to form stable complexes with transition metals. Its reactivity allows for easy alkylation of nitrogen-containing heterocycles, facilitating the construction of complex multidentate ligands.

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