2,6-Difluoro-3,5-Diiodopyridine

95%

Reagent Code: #62261
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CAS Number 685517-77-5

science Other reagents with same CAS 685517-77-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 366.87 g/mol
Formula C₅HF₂I₂N
badge Registry Numbers
MDL Number MFCD12756678
inventory_2 Storage & Handling
Storage 2-8°C, dry, airtight

description Product Description

2,6-Difluoro-3,5-diiodopyridine is primarily utilized as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine and iodine atoms, makes it highly reactive and suitable for cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential for creating complex organic molecules. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into target molecules, enhancing their metabolic stability and bioavailability. Additionally, it serves as a key intermediate in the preparation of advanced materials and specialty chemicals, where its unique halogenated pyridine core contributes to desired electronic and structural properties.

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inventory 10mg
10-20 days ฿936.00

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2,6-Difluoro-3,5-Diiodopyridine
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2,6-Difluoro-3,5-diiodopyridine is primarily utilized as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine and iodine atoms, makes it highly reactive and suitable for cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential for creating complex organic molecules. This compound is often employed in the synthesis of biologically active compounds, including potential drug can

2,6-Difluoro-3,5-diiodopyridine is primarily utilized as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure, featuring fluorine and iodine atoms, makes it highly reactive and suitable for cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential for creating complex organic molecules. This compound is often employed in the synthesis of biologically active compounds, including potential drug candidates, due to its ability to introduce fluorine atoms into target molecules, enhancing their metabolic stability and bioavailability. Additionally, it serves as a key intermediate in the preparation of advanced materials and specialty chemicals, where its unique halogenated pyridine core contributes to desired electronic and structural properties.

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