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13142-57-9

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13142-57-9 Usage

General Description

1-(3,5-dichlorophenyl)urea is a chemical compound with the molecular formula C7H6Cl2N2O. It is a white crystalline solid that is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 1-(3,5-DICHLOROPHENYL)UREA has a wide range of applications, including as an herbicide and as a precursor for the production of other chemicals. Its use as an herbicide is largely due to its ability to inhibit the growth of plants by disrupting their cell division and growth processes. Additionally, 1-(3,5-dichlorophenyl)urea is used in the production of dyes and as a corrosion inhibitor in metalworking fluids. The compound is considered to be relatively stable and has low volatility, making it an attractive choice for various industrial applications.

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 articles and documents

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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