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Urea, N'-(4-methylphenyl)-N,N-bis(phenylmethyl)-, also known as 4-methyl-N,N-bis(phenylmethyl)urea or 4-Methyl-N,N-bis(phenylmethyl)urea, is an organic compound with the chemical formula C20H21NO. It is a derivative of urea, where two phenylmethyl groups are attached to the nitrogen atom, and a 4-methylphenyl group is attached to the other nitrogen atom. Urea, N'-(4-methylphenyl)-N,N-bis(phenylmethyl)- is a white crystalline solid and is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the field of materials science, such as in the development of polymers and coatings. The compound is characterized by its unique structure, which contributes to its specific chemical properties and reactivity.

86764-30-9

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86764-30-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86764-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,6 and 4 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86764-30:
(7*8)+(6*6)+(5*7)+(4*6)+(3*4)+(2*3)+(1*0)=169
169 % 10 = 9
So 86764-30-9 is a valid CAS Registry Number.

86764-30-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dibenzyl-3-(4-methylphenyl)urea

1.2 Other means of identification

Product number -
Other names N,N-Dibenzyl-N'-p-tolyl-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:86764-30-9 SDS

86764-30-9Relevant academic research and scientific papers

A Facile and High-yielding Preparation of 1-Aryl-3,3-dialkylureas

Xian, Ming,Lu, Jianming,Zhu, Xiaoqing,Mu, Linjing,Cheng, Jin-Pei

, p. 442 - 443 (2007/10/03)

A convenient procedure for the preparation of 1-aryl-3,3-dialkylureas using bis(trichoromethyl) carbonate ('triphosgene') is described.

Transnitrosation by N-aryl-N-nitrosoureas; NO-carrying O-nitrosoisourea

Tanno,Sueyoshi,Miyata

, p. 1760 - 1767 (2007/10/02)

Transfer of nitroso groups, so-called transnitrosation, from aromatic N-nitroso compounds such as N-nitrosoureas, N-nitrosamides and N-nitrosamines, to aromatic amines or ureas was observed under non-acidic conditions at room temperature. Sterically hindered 3,3-dibenzyl-1-(4-tolyl)-1-nitrosourea (1a) rapidly nitrosates indoline, N-alkylanilines or 3-methyl-1-(4-tolyl)urea to give their N-nitroso derivatives. In the case of N,N-dimethylanilines, nitrosative demethylation occurs to give N-methyl-N-nitrosanilines. The transnitrosation is accelerated by electron-releasing groups on the nitroso acceptors, N-alkylanilines. The transnitrosation mechanism is considered to be as follows: N-nitrosourea (1) thermally decomposes to nitric oxide and ureidyl radical followed by formation of an O-nitrosoisourea intermediate (10), which acts as an NO-carrying agent and nitrosates anilines or ureas.

Potential Antiatherosclerotic Agents. 6. Hypocholesterolemic Trisubstituted Urea Analogues

DeVries, Vern G.,Bloom, Jonathan D.,Dutia, Minu D.,Katocs, Andrew S.,Largis, Elwood E.

, p. 2318 - 2325 (2007/10/02)

The discovery that a series of N,N-dialkyl-N'-arylureas were inhibitors of the ACAT enzyme has led to a structure-activity study involving the systematic modification of three sites of the urea backbone.This study culminated in the selection of N'-(2,4-dimethylphenyl)-N-benzyl-N-n-butylurea (115) for more extensive biological evaluation.ACAT inhibitors are seen as potentially beneficial agents against hypercholesterolemia and atherosclerosis.

Method of treating atherosclerosis with di(aralkyl)ureas and di(aralkyl)thioureas

-

, (2008/06/13)

Methods of treating atherosclerosis with di(aralkyl) ureas and di(aralkyl)thioureas, compositions thereof and processes for their preparation.

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