2-chloro-3-iodo-6-Methoxypyridine

95%

Reagent Code: #42150
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CAS Number 1227580-90-6

science Other reagents with same CAS 1227580-90-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.46747 g/mol
Formula C₆H₅ClINO
thermostat Physical Properties
Boiling Point 278.6±40.0 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.915±0.06 g/cm3
Storage room temperature

description Product Description

2-Chloro-3-iodo-6-methoxypyridine is primarily utilized as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the construction of complex molecules. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce pyridine-based moieties into target compounds. Additionally, it serves as a building block in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its halogenated and methoxy groups enhance reactivity, enabling precise modifications for specific applications in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿23,292.00
inventory 100mg
10-20 days ฿11,592.00

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2-chloro-3-iodo-6-Methoxypyridine
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2-Chloro-3-iodo-6-methoxypyridine is primarily utilized as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the construction of complex molecules. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce pyridine-based moieties into target compounds. Additionally, it serves as a building block in the synthesi

2-Chloro-3-iodo-6-methoxypyridine is primarily utilized as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the construction of complex molecules. The compound is often employed in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to introduce pyridine-based moieties into target compounds. Additionally, it serves as a building block in the synthesis of biologically active compounds, including potential drug candidates targeting various diseases. Its halogenated and methoxy groups enhance reactivity, enabling precise modifications for specific applications in medicinal chemistry and material science.

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