5-Iodo-2,3-difluoropyridine

95%

Reagent Code: #49288
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CAS Number 851386-35-1

science Other reagents with same CAS 851386-35-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.98 g/mol
Formula C₅H₂F₂IN
badge Registry Numbers
MDL Number MFCD09909610
thermostat Physical Properties
Melting Point 34-35 ℃
Boiling Point 206.6±35.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 2.129 g/cm3
Storage 2-8℃

description Product Description

This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile building block for the synthesis of more complex molecules. Its structure, featuring both iodine and fluorine substituents, makes it highly reactive in cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse heterocyclic compounds. These derivatives are often explored for their potential biological activities, including antimicrobial, antiviral, or anticancer properties. Additionally, it serves as a key intermediate in the development of advanced materials, particularly in the design of organic electronic components due to its electron-withdrawing characteristics. Its unique reactivity also makes it valuable in organic synthesis for constructing fluorinated pyridine derivatives, which are increasingly important in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,868.00

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5-Iodo-2,3-difluoropyridine
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This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile building block for the synthesis of more complex molecules. Its structure, featuring both iodine and fluorine substituents, makes it highly reactive in cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse heterocyclic compounds. These derivatives are often explored for their potential biological activities, including antimicrobial, antiviral, or anticancer pr

This compound is primarily utilized in the pharmaceutical and agrochemical industries as a versatile building block for the synthesis of more complex molecules. Its structure, featuring both iodine and fluorine substituents, makes it highly reactive in cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse heterocyclic compounds. These derivatives are often explored for their potential biological activities, including antimicrobial, antiviral, or anticancer properties. Additionally, it serves as a key intermediate in the development of advanced materials, particularly in the design of organic electronic components due to its electron-withdrawing characteristics. Its unique reactivity also makes it valuable in organic synthesis for constructing fluorinated pyridine derivatives, which are increasingly important in drug discovery and material science.

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