40029-93-4

Basic information

• Product Name: 2-FURAN-2-YL-4,5-DIHYDRO-1H-IMIDAZOLE
• Synonyms: ASINEX-REAG BAS 00087895;2-FURAN-2-YL-4,5-DIHYDRO-1H-IMIDAZOLE
• CAS NO: 40029-93-4
• Molecular Formula: C₇H₈N₂O
• Molecular Weight: 136.15
• Mol File: 40029-93-4.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-FURAN-2-YL-4,5-DIHYDRO-1H-IMIDAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FURAN-2-YL-4,5-DIHYDRO-1H-IMIDAZOLE(40029-93-4)
• EPA Substance Registry System: 2-FURAN-2-YL-4,5-DIHYDRO-1H-IMIDAZOLE(40029-93-4)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 40029-93-4(Hazardous Substances Data)

Usage

Synthesis Reference(s)

Tetrahedron, 47, p. 9901, 1991 DOI: 10.1016/S0040-4020(01)80726-2

Upstream product

• 139214-99-6 2-(2-furyl)-3,4,4-trimethyloxazolinium iodide 
• 107-15-3 ethylenediamine 
• 83286-30-0 2-(2-furyl)-4,5-dihydro-4,4-dimethyl-1,3-oxazole 
• 617-90-3 2-furancarbonitrile 
• 527-69-5 2-furancarbonyl chloride 
• 88-14-2 2-furanoic acid 
• 83286-35-5 N-(1,1-dimethyl-2-hydroxyethyl)furan-2-carboxamide 
• 611-13-2 2-furoic acid methyl ester 
• 98-01-1 furfural 

Downstream Products

• 139215-10-4 α-phenyl-2-<(4,5-dihydroimidazol-2-yl)furan>-3-methanol 
• 139215-09-1 α,α-diphenyl-2-<(4,5-dihydroimidazol-2-yl)furan>-3-methanol 
• 89795-49-3 2-(2-furyl)imidazole 
• 127702-53-8 1-methyl-2-(5-bromo-2-furyl)imidazole 
• 127702-55-0 1-methyl-2-(5-formyl-2-furyl)imidazole 
• 1375748-23-4 C₁₄H₁₀FN₃O 
• 1375748-21-2 C₁₇H₁₄N₄O 
• 1440421-59-9 C₁₄H₁₂N₂O₃S 
• 1440421-36-2 C₁₄H₁₄N₂O₃S 

Relevant articles and documents

Unexpected tandem condensation of 2-furonitriles with diethylenetriamine

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Efficient synthesis of 2-imidazolines in the presence of molecular iodine under ultrasound irradiation

An efficient one-pot synthesis process for preparing 2-imidazolines from aldehydes and ethylenediamine using molecular iodine and potassium carbonate in absolute ethanol at 25-30°C under ultrasound irradiation is described. The synthetic strategy has the following advantages: mild conditions and low costs requirements, readily available catalyst, short reaction times, simplicity of operation, and good-to-excellent yields.

Novel diversely substituted 1-heteroaryl-2-imidazolines for fragment-based drug discovery

A palladium-catalyzed Buchwald-Hartwig arylation protocol has been applied to achieve high-yielding N-heteroarylation of a diverse set of privileged 2-imidazolines. The resulting compounds are of interest as a novel type of molecular tool for fragment-bas