4-Chloro-6-iodoquinoline-3-carbonitrile

≥95%

Reagent Code: #119174
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CAS Number 214483-20-2

science Other reagents with same CAS 214483-20-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 314.51 g/mol
Formula C₁₀H₄ClIN₂
thermostat Physical Properties
Boiling Point 423.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

4-Chloro-6-iodoquinoline-3-carbonitrile is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of quinoline derivatives. These derivatives are often explored for their potential therapeutic properties, including antimicrobial, anticancer, and anti-inflammatory activities. The presence of both chloro and iodo substituents on the quinoline ring makes it a versatile building block for further functionalization, enabling the creation of complex molecules for drug discovery. Additionally, its unique structure allows for applications in material science, particularly in the design of organic semiconductors and fluorescent probes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,934.00
inventory 250mg
10-20 days ฿5,859.00

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4-Chloro-6-iodoquinoline-3-carbonitrile
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4-Chloro-6-iodoquinoline-3-carbonitrile is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of quinoline derivatives. These derivatives are often explored for their potential therapeutic properties, including antimicrobial, anticancer, and anti-inflammatory activities. The presence of both chloro and iodo substituents on the quinoline ring makes it a versatile bui

4-Chloro-6-iodoquinoline-3-carbonitrile is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly in the synthesis of quinoline derivatives. These derivatives are often explored for their potential therapeutic properties, including antimicrobial, anticancer, and anti-inflammatory activities. The presence of both chloro and iodo substituents on the quinoline ring makes it a versatile building block for further functionalization, enabling the creation of complex molecules for drug discovery. Additionally, its unique structure allows for applications in material science, particularly in the design of organic semiconductors and fluorescent probes.

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