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Urea, N-(4-methylphenyl)-N'-(phenylmethoxy)-, also known as 4-methylphenyl-N-phenylmethoxyurea, is an organic compound with the chemical formula C15H16N2O. It is a derivative of urea, featuring a 4-methylphenyl group attached to the nitrogen atom and a phenylmethoxy group attached to the other nitrogen atom. Urea, N-(4-methylphenyl)-N'-(phenylmethoxy)- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for the formation of different chemical bonds and reactions, making it a valuable component in the development of new compounds with specific properties and applications.

51457-92-2

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51457-92-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51457-92-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,5 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 51457-92:
(7*5)+(6*1)+(5*4)+(4*5)+(3*7)+(2*9)+(1*2)=122
122 % 10 = 2
So 51457-92-2 is a valid CAS Registry Number.

51457-92-2Relevant academic research and scientific papers

Synthesis and SAR of 1-hydroxy-1 H -benzo[ d ]imidazol-2(3 H)-ones as inhibitors of d -amino acid oxidase

Berry, James F.,Rais, Rana,Slusher, Barbara S.,Tsukamoto, Takashi,Ferraris, Dana V.,Duvall, Bridget,Hin, Niyada,Alt, Jesse,Thomas, Ajit G.,Rojas, Camilo,Hashimoto, Kenji

supporting information, p. 839 - 843,5 (2020/09/15)

A series of 1-hydroxy-1H-benzo[d]imidazol-2(3H)-ones were synthesized and evaluated for their ability to inhibit human and porcine forms of d-amino acid oxidase (DAAO). The inhibitory potency is largely dependent on the size and position of substituents o

N-substituted hydroxyureas as urease inhibitors

Uesato, Shinichi,Hashimoto, Yuichiro,Nishino, Masaru,Nagaoka, Yasuo,Kuwajima, Hiroshi

, p. 1280 - 1282 (2007/10/03)

In order to seek a urease inhibitor more potent than hydroxyurea (1), its alkyl- or phenyl-substituted derivatives were synthesized and evaluated for their effect on the jack bean urease. Of 16 compounds tested, m-methyl-(10) and m-methoxy-phenyl substituted hydroxyurea (13) showed the most potent inhibitory activities against the enzyme.

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