4-Iodo-2-methyl-1-trityl-1H-imidazole

95%

Reagent Code: #199775
fingerprint
CAS Number 157255-72-6

science Other reagents with same CAS 157255-72-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 450.32 g/mol
Formula C₂₃H₁₉IN₂
thermostat Physical Properties
Boiling Point 491°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based drugs. Its trityl-protected structure makes it valuable in solid-phase organic synthesis and peptide chemistry, where selective protection and deprotection are required. The iodo functional group allows for further modification via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for creating libraries of bioactive molecules and in the preparation of antifungal, anticancer, and antimicrobial agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,760.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Iodo-2-methyl-1-trityl-1H-imidazole
No image available
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based drugs. Its trityl-protected structure makes it valuable in solid-phase organic synthesis and peptide chemistry, where selective protection and deprotection are required. The iodo functional group allows for further modification via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemist
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of imidazole-based drugs. Its trityl-protected structure makes it valuable in solid-phase organic synthesis and peptide chemistry, where selective protection and deprotection are required. The iodo functional group allows for further modification via cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of complex heterocyclic systems. Commonly employed in medicinal chemistry for creating libraries of bioactive molecules and in the preparation of antifungal, anticancer, and antimicrobial agents.
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...