3-Iodo-2-methoxyisonicotinonitrile

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Reagent Code: #65604
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CAS Number 908279-57-2

science Other reagents with same CAS 908279-57-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.03 g/mol
Formula C₇H₅IN₂O
badge Registry Numbers
MDL Number MFCD09056806
thermostat Physical Properties
Melting Point 163-164°C
inventory_2 Storage & Handling
Storage 2-8°C

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 molecules. Its structure, featuring both an iodo and a nitrile group, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira couplings, which are essential in the construction of pharmaceuticals and agrochemicals. Additionally, the methoxy group enhances its reactivity and selectivity in various chemical transformations, making it a useful building block in medicinal chemistry for the design of drug candidates. Its applications also extend to materials science, where it can be employed in the synthesis of advanced organic materials with potential uses in electronics and optoelectronics.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,277.00
inventory 250mg
10-20 days ฿6,903.00

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3-Iodo-2-methoxyisonicotinonitrile
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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 molecules. Its structure, featuring both an iodo and a nitrile group, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira couplings, which are essential in the construction of pharmaceuticals and agrochemicals. Additionally, the methoxy group enhances its reactivity and selectivity in various chemical transfo
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure, featuring both an iodo and a nitrile group, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira couplings, which are essential in the construction of pharmaceuticals and agrochemicals. Additionally, the methoxy group enhances its reactivity and selectivity in various chemical transformations, making it a useful building block in medicinal chemistry for the design of drug candidates. Its applications also extend to materials science, where it can be employed in the synthesis of advanced organic materials with potential uses in electronics and optoelectronics.
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