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N-(thiophen-2-methyl)-N’-phenylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

100142-49-2

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100142-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100142-49-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,4 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 100142-49:
(8*1)+(7*0)+(6*0)+(5*1)+(4*4)+(3*2)+(2*4)+(1*9)=52
52 % 10 = 2
So 100142-49-2 is a valid CAS Registry Number.

100142-49-2Downstream Products

100142-49-2Relevant academic research and scientific papers

Pd/C-Catalyzed Domino Synthesis of Urea Derivatives Using Chloroform as the Carbon Monoxide Source in Water

Wang, Liang,Wang, Hao,Li, Guiqing,Min, Shuliang,Xiang, Fangyuan,Liu, Shiqi,Zheng, Waigang

, p. 4585 - 4593 (2018)

A Pd/C-catalyzed domino synthesis of symmetrical and unsymmetrical ureas from aryl iodides, sodium azide, amines and CHCl3 in water has been developed. This reaction proceeds with sequential carbonylation, Curtius rearrangement and nucleophilic addition. CHCl3 serves as a convenient and safe alternation of CO gas in the presence of KOH. A series of urea derivatives were obtained in moderate to good yields with good functional group tolerance. Furthermore, the Pd/C catalyst could be readily recovered with slight decrease in the catalytic activity after six consecutive runs. (Figure presented.).

Biochemical and microbiological evaluation of: N-aryl urea derivatives against mycobacteria and mycobacterial hydrolases

Vartak, Abhishek,Goins, Christopher,De Moura, Vinicius Calado Nogueira,Schreidah, Celine M.,Landgraf, Alexander D.,Lin, Boren,Du, Jianyang,Jackson, Mary,Ronning, Donald R.,Sucheck, Steven J.

, p. 1197 - 1204 (2019)

A focused library of 24 N-aryl urea derivatives was prepared and evaluated against serine esterases of Mycobacterium tuberculosis (Mtb) Rv3802c and Mtb Ag85C. The members of the library were evaluated for both selectivity and mode of inhibition. Furan-bas

Synthesis method of substituted urea compound

-

Paragraph 0034-0039; 0108-0113, (2021/03/31)

The invention discloses a synthesis method of a substituted urea compound, which comprises the following steps: stirring aldehyde, N-aryl urea, trichlorosilane and Lewis base in an organic solvent ata temperature range of -20 DEG C to room temperature for

Photocatalyzed synthesis of unsymmetrical ureas via the oxidative decarboxylation of oxamic acids with PANI-g-C3N4-TiO2 composite under visible light

Wang, Liang,Wang, Hao,Wang, Yaoyao,Shen, Minggui,Li, Shubai

supporting information, (2020/04/28)

The synthesis of unsymmetrical ureas via the photocatalyzed oxidative decarboxylation of oxamic acids has been developed. The carbamoyl radicals were generated from oxamic acids in the presence of a hypervalent iodine reagent and the PANI(Polyaniline)-g-C3N4-TiO2 composite under visible light irradiation. The radicals were converted in situ into the corresponding isocyanates, which were then trapped by amines to afford the corresponding products in moderate to good yields. This protocol avoided the direct use of environmentally unfriendly isocyanates and a series of substrates were tolerated. Moreover, the photocatalyst could be readily recovered by simple filtration and be reused for several runs with only a slight decrease in the catalytic activity.

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