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N'-(4-iodophenyl)-N-methyl-N-phenylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112449-24-8

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112449-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112449-24-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,4,4 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112449-24:
(8*1)+(7*1)+(6*2)+(5*4)+(4*4)+(3*9)+(2*2)+(1*4)=98
98 % 10 = 8
So 112449-24-8 is a valid CAS Registry Number.

112449-24-8SDS

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 3-(4-iodophenyl)-1-methyl-1-phenylurea

1.2 Other means of identification

Product number -
Other names N'-(4-Jod-phenyl)-N-methyl-N-phenyl-harnstoff

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:112449-24-8 SDS

112449-24-8Downstream Products

112449-24-8Relevant academic research and scientific papers

2,2,2-Trifluroenthanol promoted synthesis of unsymmetrical ureas from dioxazolones and amines via tandem lossen rearrangement/condensation process

Li, Jian,He, Wang,Lei, Pan,Song, Jiacheng,Huo, Jiyou,Wei, Hongbo,Bai, Hongjin,Xie, Weiqing

supporting information, p. 3590 - 3600 (2021/10/07)

A 2,2,2-trifluroenthanol (TFE) promoted synthesis of unsymmetric ureas was described. This approach enabled the construction of a variety of ureas from the readily prepared and easy-to-handle dioxazolones and amines via tandem Lossen rearrangement/condensation process. The reaction featured mild conditions for the urea synthesis under metal-free conditions, which was successively applied in the scale-up synthesis of herbicides Monuro and Isoproturon.

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