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Urea, N,N''-[(4-methoxyphenyl)methylene]bis-, also known as 4,4'-(methoxymethylene)bis(urea) or 4,4'-dimethoxybenzylidene bis(urea), is an organic compound with the chemical formula C10H14N2O2. It is a white crystalline solid that is soluble in water and has a molecular weight of 194.23 g/mol. Urea, N,N''-[(4-methoxyphenyl)methylene]bis- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. 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 synthesized through the reaction of 4-methoxybenzaldehyde with urea, and its structure features a central methoxymethylene bridge connecting two urea units.

52772-80-2

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52772-80-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52772-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,7 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 52772-80:
(7*5)+(6*2)+(5*7)+(4*7)+(3*2)+(2*8)+(1*0)=132
132 % 10 = 2
So 52772-80-2 is a valid CAS Registry Number.

52772-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [(carbamoylamino)-(4-methoxyphenyl)methyl]urea

1.2 Other means of identification

Product number -
Other names Urea,N,N'-[(4-methoxyphenyl)methylene]bis

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:52772-80-2 SDS

52772-80-2Relevant academic research and scientific papers

An efficient synthesis of 4,5-diaryl-3,4-dihydropyrimidin-2(1: H)-one via a cesium carbonate-promoted direct condensation of 1-aryl-2-propanone with 1,1'-(arylmethylene)diurea

Deng, Wei,Guo, Yi-Cong,Rao, Weidong,Shen, Zhi-Liang,Song, Xuan-Di,Xu, Haiyan

, p. 30062 - 30068 (2020/10/26)

An efficient method for the synthesis of 4,5-diaryl-3,4-dihydropyrimidin-2(1H)-one by using 1,1'-(arylmethylene)diurea and 1-aryl-2-propanone as substrates was developed. The reactions proceeded efficiently in the presence of Cs2CO3 to give the desired pr

Biginelli reaction via bis-ureide intermediate in low melting mixture

Mahajan, Hitesh,Jamwal, Babita,Paul, Satya

, p. 585 - 593 (2019/09/30)

This paper deals with the study of mechanism of the Biginelli reaction using low melting mixture as solvent and catalyst. The catalytic effect of low melting mixture and the reaction mechanism is discussed on the basis of nuclear magnetic resonance (NMR)

Eco-efficiency and scalable synthesis of bisamides in deep eutectic solvent

Azizi, Najmedin,Alipour, Masoumeh

, p. 268 - 271 (2015/03/18)

Solvents define a major part of the environmental performance of processes in chemical industry and also impact on cost, safety and health issues. In order to minimize the environmental impact resulting from the use of volatile organic solvents in chemica

Synthesis and antitumor activity of some 2, 3-disubstituted quinazolin-4(3H)-ones and 4, 6- disubstituted- 1, 2, 3, 4-tetrahydroquinazolin- 2H-ones

Abdel Gawad, Nagwa M.,Georgey, Hanan H.,Youssef, Riham M.,El-Sayed, Nehad A.

experimental part, p. 6058 - 6067 (2011/01/13)

The synthesis of some new 3-substituted quinazolin-4(3H)-ones and 3,4-dihydro-quinazolin-2(1H)-one derivatives and their biological evaluation as antitumor agents using the National Cancer Institute (NCI), disease oriented antitumor screening protocol are

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