3-Chloro-6-iodo-2-(trifluoromethyl)pyridine

≥95%

Reagent Code: #44655
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CAS Number 1227515-26-5

science Other reagents with same CAS 1227515-26-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.44 g/mol
Formula C₆H₂ClF₃IN
thermostat Physical Properties
Boiling Point 236.2±35.0℃(Predicted)
inventory_2 Storage & Handling
Density 2.046±0.06g/ml(Predicted)
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both chloro and iodo substituents, makes it a versatile intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the construction of diverse pyridine derivatives. The trifluoromethyl group enhances the compound's reactivity and stability, making it valuable in the development of bioactive compounds, including potential drugs and pesticides. Additionally, it is employed in material science for creating specialized polymers and coatings with unique properties. Its applications are driven by its ability to introduce fluorine atoms into target molecules, which can improve their metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿25,002.00
inventory 250mg
10-20 days ฿10,044.00

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3-Chloro-6-iodo-2-(trifluoromethyl)pyridine
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This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both chloro and iodo substituents, makes it a versatile intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the construction of diverse pyridine derivatives. The trifluoromethyl group enhances the compound's reactivity and stability, making it valuable in the development of bioactive compounds,

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring both chloro and iodo substituents, makes it a versatile intermediate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the construction of diverse pyridine derivatives. The trifluoromethyl group enhances the compound's reactivity and stability, making it valuable in the development of bioactive compounds, including potential drugs and pesticides. Additionally, it is employed in material science for creating specialized polymers and coatings with unique properties. Its applications are driven by its ability to introduce fluorine atoms into target molecules, which can improve their metabolic stability and bioavailability.

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