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1-tert-butyl-3-(2,4-dimethylphenyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

197236-19-4

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197236-19-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 197236-19-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,2,3 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 197236-19:
(8*1)+(7*9)+(6*7)+(5*2)+(4*3)+(3*6)+(2*1)+(1*9)=164
164 % 10 = 4
So 197236-19-4 is a valid CAS Registry Number.

197236-19-4Downstream Products

197236-19-4Relevant academic research and scientific papers

Synthesis and SAR studies of potent H+/K+-ATPase and anti-inflammatory activities of symmetrical and unsymmetrical urea analogues

Rakesh, Kadalipura P.,Darshini, Nanjudappa,Vidhya, Sunnadadoddi L.,Rajesha,Mallesha, Ningegowda

, p. 1675 - 1681 (2017/06/27)

A sequence of symmetrical and unsymmetrical urea derivatives 1–24 were synthesized and characterized by standard spectroscopic techniques. The synthesized analogues were tested for their in vitro H+/K+-ATPase and anti-inflammatory activities. The majority of the compounds showed outstanding activity, compared to that of omeprazole and indomethacin, usual standard drugs of antiulcer and anti-inflammatory, respectively. In particular, hydroxy, methyl, and methoxy derivatives 13–24 were the most active compounds possessing a significant amplify for diverse substituents on the benzene ring thus, contributing positively to gastric ulcer inhibition. Compounds 1–3 and 22–24 showed excellent anti-inflammatory activity due to the presence of electron-withdrawing groups (Cl and F) on the molecule.

An unexpected reaction to methodology: An unprecedented approach to transamidation

Rakesh,Ramesha,Shantharam,Mantelingu,Mallesha

, p. 108315 - 108318 (2016/11/30)

This report describes an unprecedented protocol for the synthesis of N,N′-substituted ureas using a cross-coupling method. Mono substituted ureas were modified by an economically viable and simple method using commercially available isocyanates and sodium hydride as the reagents. In addition, the method involves no expensive metal complexes or catalysts and all reactions are carried out at room temperature. Furthermore, both symmetrical and asymmetrical ureas were successfully obtained in single step reactions with reasonable yields.

Cobalt(II)-catalyzed isocyanide insertion reaction with amines under ultrasonic conditions: A divergent synthesis of ureas, thioureas and azaheterocycles

Zhu, Tong-Hao,Xu, Xiao-Ping,Cao, Jia-Jia,Wei, Tian-Qi,Wang, Shun-Yi,Ji, Shun-Jun

supporting information, p. 509 - 518 (2014/05/20)

Cobalt(II) acetylacetonate-catalyzed isocyanide insertion reactions with amines utilizing tert-butyl hydroperoxide (TBHP) as an oxidant under ultrasound conditions have been developed, which lead to the synthesis of ureas, thioureas, as well as 2-aminoben

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