112606-55-0

Basic information

• Product Name: 2-Propenoic acid, 3-[1-(triphenylmethyl)-1H-imidazol-4-yl]-, methyl ester
• CAS NO: 112606-55-0
• Molecular Formula: C26H22N2O2
• Molecular Weight: 394.473
• Mol File: 112606-55-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-[1-(triphenylmethyl)-1H-imidazol-4-yl]-, methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-[1-(triphenylmethyl)-1H-imidazol-4-yl]-, methyl ester(112606-55-0)
• EPA Substance Registry System: 2-Propenoic acid, 3-[1-(triphenylmethyl)-1H-imidazol-4-yl]-, methyl ester(112606-55-0)

Safety Data

• Hazardous Substances Data: 112606-55-0(Hazardous Substances Data)

Upstream product

• 76-83-5 trityl chloride 
• 160073-02-9 methyl 3-(imidazol-4⁽⁵⁾-yl)-2-propenoate 
• 104-98-3 urocanic acid 

Downstream Products

• 199007-50-6 1-(1-Trityl-1H-imidazol4-yl)propen-3-ol 
• 1300748-86-0 3,7,7a,8-tetrahydro-3-trityl-5H-furo[3,4-f]benzimidazol-5-one 
• 1300749-15-8 C₂₈H₂₂N₂O 
• 1300748-85-9 C₂₈H₂₄N₂O 
• 1300748-84-8 (2E)-3-(1-trityl-1H-imidazol-4-yl)prop-2-enyl propynoate 
• 1300748-83-7 (E)-3-(1-triphenylmethylimidazol-4-yl)-2-propenyl 2-propynyl ether 
• 1300748-82-6 (E)-3-(1-triphenylmethylimidazol-4-yl)-2-propenyl (E)-3-phenyl-2-propenoate 
• 1300748-81-5 (E)-3-(1-triphenylmethylimidazol-4-yl)-2-propenyl 2-propenoate 
• 1300748-80-4 (E)-3-phenyl-2-propenyl (E)-3-(1-triphenylmethylimidazol-4-yl)-2-propenyl ether 
• 1300748-79-1 (E)-3-(1-triphenylmethylimidazol-4-yl)-2-propenyl 2-propenyl ether 
• 501010-03-3 C₂₅H₃₅N₅O₄ 
• 500782-81-0 C₄₄H₄₉N₅O₄ 
• 500782-80-9 C₃₆H₃₆N₄O 
• 500782-79-6 C₄₄H₃₈N₄O₃ 

Relevant articles and documents

Intramolecular Diels-Alder chemistry of 4-vinylimidazoles

An investigation of 4-vinylimidazoles as diene components in the intramolecular Diels-Alder reaction is described. In the course of these studies several parameters affecting the cycloaddition were evaluated including the nature of the imidazole protecting group, the type of dienophile and the linking group. These investigations established that amino linkers were generally more effective than either ethers or esters. In most cases, the cycloadditions were highly stereoselective, resulting in the formation of products derived from an anti transition state. The polysubstituted tetrahydrobenzimidazole core of the pyrrole-imidazole alkaloid ageliferin can be constructed through the use of pseudo dimeric 4-vinylimidazoles.