4-Bromo-2-(methylsulfonyl)pyridine

95%

Reagent Code: #47358
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CAS Number 1209459-93-7

science Other reagents with same CAS 1209459-93-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.0900 g/mol
Formula C₆H₆NO₂SBr
badge Registry Numbers
MDL Number MFCD14702650
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of potential drug candidates, especially those targeting neurological disorders and cancer. Additionally, it is employed in organic synthesis for constructing complex pyridine derivatives, which are essential in medicinal chemistry. The compound’s reactivity and stability make it suitable for use in cross-coupling reactions, aiding in the development of novel therapeutic agents.

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inventory 100mg
10-20 days ฿6,948.00

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4-Bromo-2-(methylsulfonyl)pyridine
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Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of potential drug candidates, especially those targeting neurological disorders and cancer. Additionally, it is employed in organic synthesis for constructing complex pyridine derivatives, which are essential in medicinal chemistry. The compound’s reactivity and stability make it suitable for

Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure is particularly valuable in the creation of potential drug candidates, especially those targeting neurological disorders and cancer. Additionally, it is employed in organic synthesis for constructing complex pyridine derivatives, which are essential in medicinal chemistry. The compound’s reactivity and stability make it suitable for use in cross-coupling reactions, aiding in the development of novel therapeutic agents.

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