Methyl 2-iodoisonicotinate

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Reagent Code: #66905
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CAS Number 134579-47-8

science Other reagents with same CAS 134579-47-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.03 g/mol
Formula C₇H₆INO₂
badge Registry Numbers
MDL Number MFCD08235123
thermostat Physical Properties
Boiling Point 305.6℃ at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Methyl 2-iodoisonicotinate is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of various bioactive compounds and drug candidates. Its iodine substituent makes it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating complex molecular structures. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are often explored for their potential therapeutic properties. Its ester group also allows for further functionalization, making it versatile in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,431.00
inventory 250mg
10-20 days ฿2,862.00
inventory 1g
10-20 days ฿7,146.00
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Methyl 2-iodoisonicotinate
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Methyl 2-iodoisonicotinate is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of various bioactive compounds and drug candidates. Its iodine substituent makes it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating complex molecular structures. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are often explor

Methyl 2-iodoisonicotinate is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of various bioactive compounds and drug candidates. Its iodine substituent makes it a valuable building block for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential for creating complex molecular structures. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are often explored for their potential therapeutic properties. Its ester group also allows for further functionalization, making it versatile in medicinal chemistry research.

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