5-Iodo-1,4-dimethyl-1H-1,2,3-triazole

≥95%

Reagent Code: #49282
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CAS Number 1346818-62-9

science Other reagents with same CAS 1346818-62-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.02 g/mol
Formula C₄H₆IN₃
badge Registry Numbers
MDL Number MFCD28962625
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the construction of more complex molecules. Its unique structure, featuring both an iodine atom and a triazole ring, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the iodine atom allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researchers also explore its use in the development of fluorescent probes and imaging agents, leveraging the triazole moiety's ability to interact with biological systems. Its applications extend to material science, where it contributes to the synthesis of advanced polymers and coordination compounds with tailored properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿15,084.00
inventory 100mg
10-20 days ฿7,542.00

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5-Iodo-1,4-dimethyl-1H-1,2,3-triazole
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This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the construction of more complex molecules. Its unique structure, featuring both an iodine atom and a triazole ring, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the iodine atom allows for further functionalizati

This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile building block for the construction of more complex molecules. Its unique structure, featuring both an iodine atom and a triazole ring, makes it particularly valuable in cross-coupling reactions, such as the Suzuki-Miyaura and Sonogashira reactions, which are essential in the development of pharmaceuticals and agrochemicals. Additionally, the presence of the iodine atom allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Researchers also explore its use in the development of fluorescent probes and imaging agents, leveraging the triazole moiety's ability to interact with biological systems. Its applications extend to material science, where it contributes to the synthesis of advanced polymers and coordination compounds with tailored properties.

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