3034-62-6

Basic information

• Product Name: 2-Iodoimidazole
• Synonyms: 2-IODOIMIDAZOLE;2-lodo-1H-imidazole;2-Iodo-1H-imidazole
• CAS NO: 3034-62-6
• Molecular Formula: C₃H₃IN₂
• Molecular Weight: 193.97
• Product Categories: blocks;Imidazoles;Iodides;Heterocycles series;Halides;Imidazoles & Benzimidazoles;Imidazol&Benzimidazole;Imidaxoles;Imidazoles & Benzimidazoles;Halogenated Heterocycles;Heterocyclic Building Blocks;ImidazolesBuilding Blocks
• Mol File: 3034-62-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 182-186°C
• Boiling Point: 299.3°Cat760mmHg
• Flash Point: 134.8°C
• Appearance: /
• Density: 2.335g/cm³
• Vapor Pressure: 0.0012mmHg at 25°C
• Refractive Index: 1.688
• Storage Temp.: Keep Cold
• PKA: 11.46±0.10(Predicted)
• Sensitive: Light Sensitive
• CAS DataBase Reference: 2-Iodoimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Iodoimidazole(3034-62-6)
• EPA Substance Registry System: 2-Iodoimidazole(3034-62-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 22-24/25
• WGK Germany: 3
• Hazardous Substances Data: 3034-62-6(Hazardous Substances Data)

Usage

Uses

Reactant involved in:Alkylation leading to alkyl derivatives with antibacterial activityIodination of N-tritylimidazolePhotochemical intramolecular aromatic substitutionsSynthesis of cyclopentapyrazines using thermolysis

InChI:InChI=1/C3H3IN2/c4-3-5-1-2-6-3/h1-2H,(H,5,6)

Upstream product

• 15469-97-3 N-tritylimidazole 
• 67478-46-0 2-iodo-1-triphenylmethylimidazole 
• 288-32-4 1H-imidazole 
• 1746-25-4 2,4,5-triiodoimidazole 
• 64-17-5 ethanol 

Downstream Products

• 192804-81-2 4-[4-(2-iodo-1H-imidazol-1-yl)butyl]phenylacetic acid 
• 486999-96-6 2-iodo-1-(phenylethynyl)-1H-imidazole 
• 750647-91-7 2-iodo-1-(2-(trimethylsilyl)ethynyl)-1H-imidazole 
• 936216-53-4 2-iodo-1-(1-methyl-1-phenylethyl)-1H-imidazole 
• 135773-25-0 4-iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide 

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.

A comparison of microwave-accelerated and conventionally heated iodination reactions of some arenes and heteroarenes, using ortho-periodic acid as the oxidant

A fast and simple method for the oxidative iodination of some activated arenes and heteroarenes, either under microwave irradiation or by conventional heating, is reported, using diiodine and ortho-periodic acid as the oxidant. The reactions were carried out in hot 95% ethanol under a reflux condenser. For the microwave assisted reactions, the reaction times were always notably shortened, but the yields were nearly the same as those afforded by the conventional method.