5675-04-7

Basic information

• Product Name: 1-benzyl-2-(3-bromophenyl)-3-{[(1E)-1-(4-chlorophenyl)ethylidene]amino}imidazolidin-4-one
• CAS NO: 5675-04-7
• Molecular Formula: C₄H₁₀O₂S
• Molecular Weight: 482.8
• Mol File: 5675-04-7.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 562.3°C at 760 mmHg
• Flash Point: 293.9°C
• Density: 1.38g/cm³
• Vapor Pressure: 1.14E-12mmHg at 25°C
• Refractive Index: 1.645
• CAS DataBase Reference: 1-benzyl-2-(3-bromophenyl)-3-{[(1E)-1-(4-chlorophenyl)ethylidene]amino}imidazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-2-(3-bromophenyl)-3-{[(1E)-1-(4-chlorophenyl)ethylidene]amino}imidazolidin-4-one(5675-04-7)
• EPA Substance Registry System: 1-benzyl-2-(3-bromophenyl)-3-{[(1E)-1-(4-chlorophenyl)ethylidene]amino}imidazolidin-4-one(5675-04-7)

Safety Data

• Hazardous Substances Data: 5675-04-7(Hazardous Substances Data)

Upstream product

• 7559-57-1 n-butyl α-disulfone 
• 80-15-9 Cumene hydroperoxide 
• 78518-71-5 1-anilino-2-butylthio-3-butoxypropane 

Downstream Products

• 1509939-23-4 (E)-(3-(butylsulfonyl)prop-1-en-1-yl)benzene 
• 20129-23-1 butyl phenyl disulfide 
• 882-33-7 diphenyldisulfane 
• 2386-47-2 butane-1-sulfonic acid 
• 629-45-8 dibutyl disulfide 
• 117379-80-3 C₈H₁₈O₂S₂ 
• 1118-40-7 S-butyl butanethiosulfonate 
• 73663-90-8 (Z)-ethyl 3-(butylsulfonyl)acrylate 
• 73663-90-8 (E)-ethyl 3-(butylsulfonyl)acrylate 

Relevant articles and documents

The Mechanism of Antioxidative Action of Substituted 1,2-Aminopropanethiols in Oxidation of Cumene

The influence of substituted 1,2-aminopropanethiols on cumene oxidation was studied, and they were shown to be effective oxidation inhibitors. It was found that these compounds are inhibitors of combined action: they terminate the oxidation chain by the reaction with peroxide radicals and, being oxidized by cumyl hydroperoxide, give products that catalytically decompose the peroxides. The correlation of the substituent nature in the 1,2-aminopropanethiol molecule on inhibitor reactivity in elementary reactions of inhibition of cumene oxidation was established.