4-Hydroxy-5-iodo-2-(trifluoromethyl)pyridine

98%

Reagent Code: #119593
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CAS Number 1027818-89-8

science Other reagents with same CAS 1027818-89-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.99 g/mol
Formula C₆H₃F₃INO
inventory_2 Storage & Handling
Storage 2-8°C, sealed, protected from light

description Product Description

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex compounds. Its unique structure, featuring both iodine and trifluoromethyl groups, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The iodine atom can participate in various coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds essential for drug development. Additionally, the trifluoromethyl group enhances the metabolic stability and lipophilicity of the resulting compounds, which is crucial for improving the efficacy and bioavailability of pharmaceutical agents. Researchers also explore its potential in the synthesis of advanced materials, particularly those requiring halogenated aromatic systems for specific electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,072.00
inventory 100mg
10-20 days ฿6,228.00
inventory 1g
10-20 days ฿28,548.00

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4-Hydroxy-5-iodo-2-(trifluoromethyl)pyridine
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This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex compounds. Its unique structure, featuring both iodine and trifluoromethyl groups, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The iodine atom can participate in various coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds essential for drug development. Addition

This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex compounds. Its unique structure, featuring both iodine and trifluoromethyl groups, makes it particularly valuable in the creation of pharmaceuticals and agrochemicals. The iodine atom can participate in various coupling reactions, such as Suzuki or Sonogashira couplings, enabling the formation of carbon-carbon bonds essential for drug development. Additionally, the trifluoromethyl group enhances the metabolic stability and lipophilicity of the resulting compounds, which is crucial for improving the efficacy and bioavailability of pharmaceutical agents. Researchers also explore its potential in the synthesis of advanced materials, particularly those requiring halogenated aromatic systems for specific electronic or optical properties.

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