Ethyl 4-iodo-1-(4-methoxybenzyl)-1H-pyrazole-3-carboxylate

97%

Reagent Code: #86171
fingerprint
CAS Number 1355249-29-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.19 g/mol
Formula C₁₄H₁₅IN₂O₃
badge Registry Numbers
MDL Number MFCD30180245
thermostat Physical Properties
Boiling Point 464.2±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed away from light

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the construction of heterocyclic compounds, particularly pyrazole derivatives, which are of significant interest in medicinal chemistry. The presence of the iodine atom makes it a valuable substrate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of various functional groups or aromatic systems. Additionally, the methoxybenzyl group provides stability and can influence the reactivity of the molecule in further transformations. Its applications extend to the synthesis of potential pharmaceutical agents, including inhibitors or modulators of biological targets, due to the versatility of the pyrazole core in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days $403.90
inventory 100mg
10-20 days $201.95
Ethyl 4-iodo-1-(4-methoxybenzyl)-1H-pyrazole-3-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. It is often employed in the construction of heterocyclic compounds, particularly pyrazole derivatives, which are of significant interest in medicinal chemistry. The presence of the iodine atom makes it a valuable substrate for cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the introduction of various functional groups or aromatic systems. Additionally, the methoxybenzyl group provides stability and can influence the reactivity of the molecule in further transformations. Its applications extend to the synthesis of potential pharmaceutical agents, including inhibitors or modulators of biological targets, due to the versatility of the pyrazole core in drug discovery.
Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...

Cart

No products

Subtotal: $0.00
Total $0.00 AUD