Ethyl 4-iodo-1H-pyrazole-5-carboxylate

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Reagent Code: #183548
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CAS Number 179692-08-1

science Other reagents with same CAS 179692-08-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.04 g/mol
Formula C₆H₇IN₂O₂
badge Registry Numbers
MDL Number MFCD00466329
thermostat Physical Properties
Boiling Point 345.6±22.0°C at N/A mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building pyrazole-based bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing novel pesticides with improved activity and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿154.00
inventory 5g
10-20 days ฿1,800.00
inventory 10g
10-20 days ฿3,330.00
inventory 25g
10-20 days ฿7,570.00
inventory 1g
10-20 days ฿570.00

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Ethyl 4-iodo-1H-pyrazole-5-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building pyrazole-based bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and antiviral agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for building pyrazole-based bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the creation of diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing novel pesticides with improved activity and selectivity.

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