Methyl 4-iodo-1H-pyrazole-3-carboxylate

98%

Reagent Code: #208785
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CAS Number 136944-79-1

science Other reagents with same CAS 136944-79-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.01 g/mol
Formula C₅H₅IN₂O₂
badge Registry Numbers
MDL Number MFCD09473436
thermostat Physical Properties
Boiling Point 338.5±22.0°C at 760 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, antiviral agents, antimicrobials, and anti-inflammatory drugs. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the creation of complex heterocyclic compounds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and stability in various synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿830.00
inventory 250mg
10-20 days ฿1,210.00
inventory 1g
10-20 days ฿4,820.00
inventory 5g
10-20 days ฿20,240.00
inventory 25g
10-20 days ฿70,840.00

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Methyl 4-iodo-1H-pyrazole-3-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors, antiviral agents, antimicrobials, and anti-inflammatory drugs. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the creation of complex heterocyclic compounds. Also utilized in agrochem

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors, antiviral agents, antimicrobials, and anti-inflammatory drugs. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building bioactive molecules. Commonly employed in cross-coupling reactions, such as Suzuki or Heck reactions, to introduce aryl or vinyl groups, enabling the creation of complex heterocyclic compounds. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and stability in various synthetic pathways.

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