5873-91-6

Basic information

• Product Name: 1-(4-tert-butylbenzyl)-3-(4-ethylphenyl)-1-(1-phenylethyl)urea
• CAS NO: 5873-91-6
• Molecular Formula: C₈H₈S₂
• Molecular Weight: 414.5824
• Mol File: 5873-91-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 588°C at 760 mmHg
• Flash Point: 309.4°C
• Density: 1.078g/cm³
• Vapor Pressure: 8.34E-14mmHg at 25°C
• Refractive Index: 1.593
• CAS DataBase Reference: 1-(4-tert-butylbenzyl)-3-(4-ethylphenyl)-1-(1-phenylethyl)urea(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-tert-butylbenzyl)-3-(4-ethylphenyl)-1-(1-phenylethyl)urea(5873-91-6)
• EPA Substance Registry System: 1-(4-tert-butylbenzyl)-3-(4-ethylphenyl)-1-(1-phenylethyl)urea(5873-91-6)

Safety Data

• Hazardous Substances Data: 5873-91-6(Hazardous Substances Data)

Upstream product

• 103-80-0 phenylacetyl chloride 
• 75-15-0 carbon disulfide 
• 100-44-7 benzyl chloride 
• 463-58-1 carbon oxide sulfide 
• 1589-82-8 phenylmagnesium bromide 
• 20568-14-3 Dithiophenylessigsaeure-ethylester 
• 6921-34-2 benzylmagnesium chloride 

Downstream Products

• 69200-91-5 phenyl-acetaldehyde phenylhydrazone 
• 20185-00-6 1-phenyl-2-phenylthioacetylhydrazine 
• 500791-38-8 (2-phenyl-thioacetylamino)-malonic acid diethyl ester 
• 10593-79-0 Phenylacetothiohydroxamic Acid 
• 7028-48-0 Phenylacetaldehyde oxime 
• 140-29-4 phenylacetonitrile 
• 858843-30-8 phenyl-thioacetic acid-(N-methyl-N'-phenyl-hydrazide) 
• 872808-70-3 phenylthioacetylglycine 
• 15985-67-8 N-phenylthioacetyl-valine 
• 101956-05-2 N-phenylthioacetyl-DL-isoleucine 
• 872808-41-8 3,3-diethoxy-2-(2-phenyl-thioacetylamino)-propionic acid 
• 96196-98-4 phenyl-thioacetic acid furfurylidenehydrazide 
• 54829-40-2 S-benzyl-2-phenylethanethioate 

Relevant articles and documents

Design criteria for star polymer formation processes via living free radical polymerization

The kinetics of reversible addition-fragmentation chain transfer (RAFT), R-group approach star polymerizations have been studied via a combined experimental and theoretical approach. From the improved understanding herein developed, design criteria have been suggested to aid in future syntheses of RAFT, R-group approach star polymer. The suggested criteria are as follows. To minimize the quantity of linear polymer in the system, it is important to have a high rate of monomer propagation but a small delivery of radicals to the system. Crucial to the prevention of star-star coupling and resulting molecular weight distribution (MWD) broadening is the minimization of radical termination events between star molecules. Noting that the number of termination events is directly correlated to the number of decomposed initiator molecules, this might be achieved via several methods. A slow rate of initiator decomposition, a fast rate of propagation, or use of a rate-retarding RAFT agent can all lead to a reduction in star-star coupling events. Additionally, simulations reported herein demonstrate that the use of a star-forming RAFT agent substrate which has a fewer number of arms will lead to a reduction in the concentration of star-star coupled products. Ab initio calculations have been used to study intramolecular RAFT equilibria occurring early in the preequilibrium. These calculations have shown that highly stable intramolecular adduct radicals might be formed due to the close proximity of radicals and S=C bonds. The effect of these on the kinetics is studied.

Ambient temperature reversible addition-fragmentation chain transfer polymerisation

Reversible addition fragmentation chain transfer was performed at ambient temperature for the first time.