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Urea, N-[4-(dimethylamino)phenyl]-N'-phenyl-, also known as N,N'-(4-dimethylaminophenyl)-N-phenylurea or 4-dimethylaminophenyl-phenylurea, is an organic compound with the chemical formula C15H16N2O. It is a derivative of urea, featuring a urea group (-NH2-CO-NH2) and two phenyl rings, one of which is substituted with a dimethylamino group (-N(CH3)2). Urea, N-[4-(dimethylamino)phenyl]-N'-phenyl- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. Its structure and properties make it a versatile building block in organic chemistry, allowing for the creation of a wide range of compounds with different applications.

13143-07-2

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13143-07-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13143-07-2 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 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13143-07:
(7*1)+(6*3)+(5*1)+(4*4)+(3*3)+(2*0)+(1*7)=62
62 % 10 = 2
So 13143-07-2 is a valid CAS Registry Number.

13143-07-2SDS

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-phenyl-3[4-(N,N-dimethylamino)phenyl]urea

1.2 Other means of identification

Product number -
Other names N-(4-(DIMETHYLAMINO)PHENYL)-N'-PHENYLUREA

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:13143-07-2 SDS

13143-07-2Relevant academic research and scientific papers

METHODS OF INHIBITING BACTERIAL VIRULENCE AND COMPOUNDS RELATING THERETO

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Paragraph 0165, (2017/01/31)

The present invention relates to compounds and methods for the treatment of bacterial infections. Because their mechanism of action does not involve killing of bacteria or inhibiting their growth, the potential for these compounds to induce drug resistance in bacteria is minimized. Through inhibiting bacterial virulence, the present invention provides a novel means of treating bacterial infections.

Electrochemically controlled hydrogen bonding. Electrolyte effects in an oxidation-based arylurea-amide system

Woods, Jessica E.,Ge, Yu,Smith, Diane K.

supporting information; experimental part, p. 10070 - 10071 (2009/02/04)

Oxidation of a dimethylaminophenyl-substituted urea leads to a > 2000-fold increase in binding strength between the urea and a diamide guest in 0.1 M NBu4B(C6F5)4/CH2Cl2. The strength of th

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