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1-(4-aminophenyl)-2-Imidazolidinone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89518-99-0

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89518-99-0 Usage

Type

Chemical compound

Derivative of

Imidazolidinone

Industrial applications

a. Photoinitiator in UV-curable inks and coatings
b. Component in the formulation of hair dyes

Physical appearance

White to pale yellow powder

Solubility

Soluble in organic solvents such as ethanol and acetone

Potential health risk

Known for causing allergic reactions in some individuals

Safety precautions

Handle with caution and in accordance with safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 89518-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,1 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89518-99:
(7*8)+(6*9)+(5*5)+(4*1)+(3*8)+(2*9)+(1*9)=190
190 % 10 = 0
So 89518-99-0 is a valid CAS Registry Number.

89518-99-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-aminophenyl)imidazolidin-2-one

1.2 Other means of identification

Product number -
Other names -

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:89518-99-0 SDS

89518-99-0Relevant academic research and scientific papers

NOVEL IMIDAZO-PYRAZINE DERIVATIVES

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Page/Page column 45; 48-49, (2021/12/31)

The invention provides novel imidazo-pyrazine derivatives having the general formula (I), and pharmaceutically acceptable salts thereof, wherein X, m, n, and R1to R3 are as described herein: formula (I). Further provided are pharmace

Mild, convenient and versatile Cu-mediated synthesis of N-aryl-2-imidazolidinones

Stabile, Paolo,Lamonica, Alessandro,Ribecai, Arianna,Castoldi, Damiano,Guercio, Giuseppe,Curcuruto, Ornella

supporting information; experimental part, p. 3232 - 3235 (2010/08/07)

A mild, general, convenient and practical methodology for the selective copper-mediated mono N-arylation of unprotected 2-imidazolidinone was developed. Strong electron-donating groups and free hydroxy and amino groups on the aryl iodide substrates were well tolerated. The use of n-butanol as the solvent for the copper-catalysed mono-arylation of 2-imidazolidinone is unprecedented.

Heterocyclic compounds

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Page/Page column 12-13, (2010/11/26)

The present invention relates to the area of blood clotting. The invention relates in particular to certain heterocyclic compounds, to processes for their preparation, to their use for the treatment and/or prophylaxis of diseases, and to their use for pro

PYRAZINE DICARBOXAMIDES AND THE USE THEREOF

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Page/Page column 24, (2010/11/08)

The invention relates to novel pyrazine dicarboxamides, methods for the use thereof, their use for treating and/or preventing diseases as well as to their use for producing medicaments for treating and/or preventing diseases, particularly thromboembolic disorders.

HETEROCYCLIC COMPOUNDS

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Page/Page column 31, (2010/02/09)

The invention concerns blood clotting. The invention particularly concerns certain heterocyclic compounds, methods for the production thereof, their use for treating and/or preventing diseases, and their use for producing medicaments for treating and/or preventing diseases.

ANTIHYPERTENSIVE 3-(UREIDOCYCLOHEXYLENEAMINO)PROPANE-1,2-DIOL DERIVATIVES

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, (2008/06/13)

Certain 3-(ureidocyclohexyleneamino)propane-1,2-diol derivatives, such as the compounds of formula III below, represent novel and useful pharmaceutical agents, e.g. potent antihypertensive and cardioactive agents demonstrating both α-and β-adrenergic bloc

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