2-Pyridyl tribromomethyl sulfone

98%

Reagent Code: #224799
label
Alias 2-(tribromomethanesulfonyl)pyridine
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CAS Number 59626-33-4

science Other reagents with same CAS 59626-33-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.88 g/mol
Formula C₆H₄Br₃NO₂S
badge Registry Numbers
MDL Number MFCD02093493
thermostat Physical Properties
Melting Point 159-162°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a reagent in organic synthesis, particularly in radical reactions where the tribromomethyl group acts as a source of bromine radicals under thermal or photochemical conditions. It serves as a brominating agent for alkenes and alkynes, enabling selective bromination in complex molecule synthesis. Also employed in the preparation of heterocyclic compounds due to the pyridyl ring's coordinating ability, facilitating metal-catalyzed transformations. Its sulfone moiety enhances stability and solubility in polar solvents, making it suitable for use in multistep synthetic routes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿4,270.00
25g
10-20 days ฿13,750.00
2-Pyridyl tribromomethyl sulfone
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Used as a reagent in organic synthesis, particularly in radical reactions where the tribromomethyl group acts as a source of bromine radicals under thermal or photochemical conditions. It serves as a brominating agent for alkenes and alkynes, enabling selective bromination in complex molecule synthesis. Also employed in the preparation of heterocyclic compounds due to the pyridyl ring's coordinating ability, facilitating metal-catalyzed transformations. Its sulfone moiety enhances stability and solubilit

Used as a reagent in organic synthesis, particularly in radical reactions where the tribromomethyl group acts as a source of bromine radicals under thermal or photochemical conditions. It serves as a brominating agent for alkenes and alkynes, enabling selective bromination in complex molecule synthesis. Also employed in the preparation of heterocyclic compounds due to the pyridyl ring's coordinating ability, facilitating metal-catalyzed transformations. Its sulfone moiety enhances stability and solubility in polar solvents, making it suitable for use in multistep synthetic routes.

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