73955-62-1

Basic information

• Product Name: Imidazolidine, 1-acetyl-2-(4-methoxyphenyl)-3,4,4-trimethyl-
• CAS NO: 73955-62-1
• Molecular Formula: C15H22N2O2
• Molecular Weight: 262.352
• Mol File: 73955-62-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Imidazolidine, 1-acetyl-2-(4-methoxyphenyl)-3,4,4-trimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Imidazolidine, 1-acetyl-2-(4-methoxyphenyl)-3,4,4-trimethyl-(73955-62-1)
• EPA Substance Registry System: Imidazolidine, 1-acetyl-2-(4-methoxyphenyl)-3,4,4-trimethyl-(73955-62-1)

Safety Data

• Hazardous Substances Data: 73955-62-1(Hazardous Substances Data)

Upstream product

• 2305-59-1 4,4-dimethyl-2-imidazoline 
• 71254-88-1 1-acetyl-4,4-dimethyl-Δ²-imidazoline 
• 104-92-7 1-bromo-4-methoxy-benzene 
• 71254-90-5 1-acetyl-3,4,4-trimethyl-Δ²-imidazolinium iodide 

Downstream Products

• 3380-73-2 1-(4-methoxyphenyl)-1,2,3,4-tetrahydro-1H-pyrido[3,4-b]indole 

Relevant articles and documents

MODELS OF FOLATE COENZYMES-VII SYNTHESIS AND CARBON TRANSFER REACTIONS OF N5,N10-METHENYL AND N5,N10-METHYLENETETRAHYDROFOLATE MODELS

Carboxylate esters react with 1,2-diaminoethanes to yield imidazolines, which upon consecutive reaction with acetic anhydride or tosyl chloride and methyl iodide give imidazolinium salts that serve as models of N5,N10-(CH+)-tetrahydrofolate (THF) coenzymes (7a,b and 18a,b).Reduction of the latter salts with sodium borohydride or reaction with anions (R-) give the corresponding 5,10--THF models.Mono- and bifunctional nucleophiles react with 18a,b to yield carbon-transfer products. 6-Alkylamino-1,3-dimethyluracils react with 1-tosyl-3,4,4-trimethylimidazolidine (the reduction product of 18b), in the presence of acetic acid, to form carbon-transfer products via a mechanism which bears close analogy to the mechanism of action of thymidylate synthetase.