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1-(3,5-DICHLOROPHENYL)UREA is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13142-57-9

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13142-57-9 Usage

Appearance

White crystalline solid

Uses

a. Intermediate in the synthesis of pharmaceuticals and agrochemicals
b. Herbicide
c. Precursor for the production of other chemicals
d. Production of dyes
e. Corrosion inhibitor in metalworking fluids

Mechanism of action as herbicide

Inhibits plant growth by disrupting cell division and growth processes

Stability

Relatively stable

Volatility

Low volatility

Industrial applications

Attracts various industrial applications due to its stability and low volatility

Check Digit Verification of cas no

The CAS Registry Mumber 13142-57-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,4 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13142-57:
(7*1)+(6*3)+(5*1)+(4*4)+(3*2)+(2*5)+(1*7)=69
69 % 10 = 9
So 13142-57-9 is a valid CAS Registry Number.

13142-57-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3,5-Dichlorophenyl)urea

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:13142-57-9 SDS

13142-57-9Relevant academic research and scientific papers

Transition Metal-Free Carbazole Synthesis from Arylureas and Cyclohexanones

Wu, Jun,Xie, Yanjun,Chen, Xiangui,Deng, Guo-Jun

supporting information, p. 3206 - 3211 (2016/10/21)

An efficient strategy for carbazole synthesis from arylureas and cyclohexanones under transition metal-free conditions has been developed. The combined use of potassium iodide and iodine could significantly improve the reaction efficiency to provide 2,6-disubstituted 9-arylcarbazoles in moderate to good yields. In this kind of transformation, the whole carbazole moiety (except the nitrogen atom) comes from two equivalents of cyclohexanones. (Figure presented.).

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