3-Methyl-4-iodopyrazole

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Reagent Code: #205360
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CAS Number 15802-75-2

science Other reagents with same CAS 15802-75-2

blur_circular Chemical Specifications

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Weight 208 g/mol
Formula C₄H₅IN₂
badge Registry Numbers
MDL Number MFCD09908176
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, antibacterial, and insecticidal properties. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex pyrazole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the iodine atom's utility in cross-coupling reactions, such as Suzuki or Heck reactions, allowing rapid diversification of compound libraries. Also applied in the preparation of kinase inhibitors and other targeted therapies in drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿20.00
inventory 5g
10-20 days ฿430.00
inventory 25g
10-20 days ฿1,660.00

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3-Methyl-4-iodopyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, antibacterial, and insecticidal properties. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex pyrazole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the iodine atom's utility in cross-coupling reactions, such as Suzuki or Heck reactio

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, antibacterial, and insecticidal properties. Its structure serves as a building block in heterocyclic chemistry, enabling the creation of more complex pyrazole derivatives. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the iodine atom's utility in cross-coupling reactions, such as Suzuki or Heck reactions, allowing rapid diversification of compound libraries. Also applied in the preparation of kinase inhibitors and other targeted therapies in drug discovery.

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