3-Methyl-4-iodopyrazole

98%

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

scatter_plot Molecular Information
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.

Available Sizes & Pricing

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