4-Iodo-2-methylpyrazole-3-carbonitrile

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Reagent Code: #200614
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CAS Number 1354705-14-8

science Other reagents with same CAS 1354705-14-8

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scatter_plot Molecular Information
Weight 233.01 g/mol
Formula C₅H₄IN₃
badge Registry Numbers
MDL Number MFCD24539521
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, antiviral, and anti-inflammatory properties. Also employed in agrochemical research for designing new pesticides and herbicides due to its ability to enhance molecular binding and stability. Commonly utilized in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex heterocyclic systems in drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,690.00
inventory 250mg
10-20 days ฿9,590.00
inventory 1g
10-20 days ฿24,780.00

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4-Iodo-2-methylpyrazole-3-carbonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, antiviral, and anti-inflammatory properties. Also employed in agrochemical research for designing new pesticides and herbicides due to its ability to enhance molecular binding and stability. Commonly utilized in cro

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with potential anticancer, antiviral, and anti-inflammatory properties. Also employed in agrochemical research for designing new pesticides and herbicides due to its ability to enhance molecular binding and stability. Commonly utilized in cross-coupling reactions, such as Suzuki and Heck reactions, to build complex heterocyclic systems in drug discovery.

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