67478-46-0

Basic information

• Product Name: 2-Iodo-1-trityl-1H-imidazole
• Synonyms: 2-IODO-1-TRITYL-1H-IMIDAZOLE;2-Iodo-1-tritylimidazole;2-iodo-1-(triphenylMethyl)-1H-iMidazole
• CAS NO: 67478-46-0
• Molecular Formula: C22H17IN2
• Molecular Weight: 436.29
• Product Categories: blocks;Imidazoles;Iodides
• Mol File: 67478-46-0.mol
• Article Data: 3

Chemical Properties

• Melting Point: 170-171℃
• Boiling Point: 556.5 °C at 760 mmHg
• Flash Point: 290.4 °C
• Appearance: crystal
• Density: 1.4 g/cm³
• Storage Temp.: 2-8°C
• Sensitive: Light Sensitive
• CAS DataBase Reference: 2-Iodo-1-trityl-1H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Iodo-1-trityl-1H-imidazole(67478-46-0)
• EPA Substance Registry System: 2-Iodo-1-trityl-1H-imidazole(67478-46-0)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 67478-46-0(Hazardous Substances Data)

Usage

General Description

2-Iodo-1-trityl-1H-imidazole is a chemical compound with the molecular formula C23H20IN3. It is a derivative of imidazole, which is a five-membered heterocyclic ring compound. The iodo group in the molecule makes it useful as a halogenating agent in organic synthesis, while the trityl group imparts stability to the compound. It can also be used as a reagent in the synthesis of various pharmaceutical and biological compounds due to its versatile chemical properties. Additionally, 2-Iodo-1-trityl-1H-imidazole has been studied for its potential use in medicinal chemistry and drug development, making it a valuable and versatile chemical in research and industry.

Upstream product

• 15469-97-3 N-tritylimidazole 

Relevant articles and documents

FRICTIONLESS MOLECULAR ROTARY MOTORS

A rotaxane consisting of a cucurbituril and an uncharged guest molecule, having low or null affinity therebetween is provided as well as processes for providing the same. Various uses as energy converters (“frictionless” molecular motors), biochips and biosensors using the same are also provided.

Remarkable Selectivity in the Reaction of 1-Trityl-2-lithioimidazoles with t-Butyl Halogenoacetates

2-Lithio-1-triphenylmethylimidazoles react with t-butyl halogenoacetates to give a variety of products, the nature of which is cleanly determined by the halogen atom.With chloroacetate the products are chloromethyl ketones, while bromacetate gives di-t-butyl imidazolesuccinates, and iodoacetate yields iodoimidazoles.In each case 50percent of the parent triphenylmethylimidazole is recovered from the reaction.When the triphenylmethyl substituent is replaced by the N,N-dimethylsulfamoyl group, reaction with bromoacetate is suppressed, but t-butyl chloroacetate and iodoacetate again give chloroketones and aryl iodides respectively.