108412-94-8

Basic information

• Product Name: 1H-Imidazole,1-(3-butenyl)-(9CI)
• Synonyms: 1H-Imidazole,1-(3-butenyl)-(9CI)
• CAS NO: 108412-94-8
• Molecular Formula: C7H10N2
• Molecular Weight: 122.1677
• Product Categories: AMINETERTIARY
• Mol File: 108412-94-8.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Imidazole,1-(3-butenyl)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole,1-(3-butenyl)-(9CI)(108412-94-8)
• EPA Substance Registry System: 1H-Imidazole,1-(3-butenyl)-(9CI)(108412-94-8)

Safety Data

• Hazardous Substances Data: 108412-94-8(Hazardous Substances Data)

Usage

Type of compound

heterocyclic (five-membered ring with three carbon atoms and two nitrogen atoms)

Physical properties

clear, colorless liquid with a pungent odor

Solubility

insoluble in water, soluble in organic solvents

Uses

building block in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals

Safety precautions

may cause irritation to the skin, eyes, and respiratory system

Upstream product

• 288-32-4 1H-imidazole 
• 5162-44-7 1-bromo-4-butene 

Relevant articles and documents

Enantioselective synthesis of macrocyclic heterobiaryl derivatives of molecular asymmetry by molybdenum-catalyzed asymmetric ring-closing metathesis

Winding vine-shaped molecular asymmetry is induced by enantioselective ring-closing metathesis with a chiral molybdenum catalyst. The reaction proceeds under mild conditions through an E-selective ring-closing metathesis leading to macrocyclic bisazoles w

Tin-free radical sequences under acidic conditions. Convergent access to azole-containing structures

(equation presented) Various xanthates add efficiently to olefins bearing [1,2,4]triazole, imidazole, or benzimidazole moieties in the presence of camphorsulfonic acid via a radical chain reaction initiated by a small amount of lauroyl peroxide. The adducts may be transformed to more complex molecules by implementing a further radical cyclization.