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1-(4-tert-butylbenzyl)-3-(4-ethylphenyl)-1-(1-phenylethyl)urea is a complex organic compound with the molecular formula C30H36N2O. It is a derivative of urea, featuring a urea functional group (-NH-CO-NH-) and three distinct aryl substituents. The compound consists of a 4-tert-butylbenzyl group, a 4-ethylphenyl group, and a 1-phenylethyl group attached to the urea core. This chemical is characterized by its unique molecular structure, which contributes to its specific properties and potential applications in various fields, such as pharmaceuticals, agrochemicals, or materials science. Due to its complex structure, it is essential to consider the compound's stability, reactivity, and potential interactions with other molecules when studying or utilizing it in various applications.

5873-91-6

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5873-91-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5873-91-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,7 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5873-91:
(6*5)+(5*8)+(4*7)+(3*3)+(2*9)+(1*1)=126
126 % 10 = 6
So 5873-91-6 is a valid CAS Registry Number.

5873-91-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(4-tert-butylphenyl)methyl]-3-(4-ethylphenyl)-1-(1-phenylethyl)urea

1.2 Other means of identification

Product number -
Other names Phenyl-dithioessigsaeure

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5873-91-6 SDS

5873-91-6Relevant academic research and scientific papers

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

Chaffey-Millar, Hugh,Stenzel, Martina H.,Davis, Thomas P.,Coote, Michelle L.,Barner-Kowollik, Christopher

, p. 6406 - 6419 (2006)

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.

Successful use of RAFT techniques in seeded emulsion polymerization of styrene: Living character, RAFT agent transport, and rate of polymerization

Prescott, Stuart W.,Ballard, Mathew J.,Rizzardo, Ezio,Gilbert, Robert G.

, p. 5417 - 5425 (2007/10/03)

Reversible addition-fragmentation chain transfer (RAFT) polymerization techniques are successfully used to control molecular weight and polydispersity in the seeded emulsion polymerization of styrene. A novel technique was used to assist the transport int

Ambient temperature reversible addition-fragmentation chain transfer polymerisation

Quinn,Rizzardo,Davis

, p. 1044 - 1045 (2007/10/03)

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

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