3-Iodo-1-methyl-1H-pyrazole

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Reagent Code: #199705
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CAS Number 92525-10-5

science Other reagents with same CAS 92525-10-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208 g/mol
Formula C₄H₅IN₂
thermostat Physical Properties
Boiling Point 226.9°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require iodinated heterocyclic structures. Its reactivity allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic frameworks. Commonly employed in medicinal chemistry for lead optimization due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation of radiolabeled compounds for imaging and tracer studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿162.00
inventory 1g
10-20 days ฿790.00
inventory 5g
10-20 days ฿3,040.00
inventory 25g
10-20 days ฿12,550.00
inventory 100g
10-20 days ฿16,430.00

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3-Iodo-1-methyl-1H-pyrazole
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require iodinated heterocyclic structures. Its reactivity allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic frameworks. Commonly employed in medicinal chemistry for lead optimization due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the prepar

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require iodinated heterocyclic structures. Its reactivity allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex organic frameworks. Commonly employed in medicinal chemistry for lead optimization due to its ability to enhance binding affinity and metabolic stability in drug candidates. Also utilized in the preparation of radiolabeled compounds for imaging and tracer studies.

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