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Urea, N-[4-hydroxy-3-[(4-methyl-1-piperazinyl)methyl]phenyl]-N'-(4-nitrophenyl) is a complex organic compound with a molecular formula of C18H21N5O4. It is characterized by the presence of a urea group, a 4-hydroxy-3-[(4-methyl-1-piperazinyl)methyl]phenyl group, and a 4-nitrophenyl group. This chemical is known for its potential applications in pharmaceuticals, particularly as a precursor in the synthesis of certain drugs. Its structure includes a phenyl ring with a hydroxyl group and a piperazine-modified side chain, which contributes to its biological activity. The compound's properties and reactivity are influenced by the presence of the nitro group on the second phenyl ring, which can participate in various chemical reactions.

93958-40-8

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93958-40-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93958-40-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,9,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93958-40:
(7*9)+(6*3)+(5*9)+(4*5)+(3*8)+(2*4)+(1*0)=178
178 % 10 = 8
So 93958-40-8 is a valid CAS Registry Number.

93958-40-8Downstream Products

93958-40-8Relevant academic research and scientific papers

Studies in Potential Filaricides: Part XVI - Synthesis of 2,4-Disubstituted Aminophenols and Related Benzophenones as Amodiaquine Analogs

Agrawal, V. K.,Sharma, Satyavan

, p. 839 - 843 (2007/10/02)

A series of 2,4-disubstituted aminophenols (6-16, 18, 19, 22, 25) and substituted benzophenones (17, 20, 21, 23, 24, 33-35) and benzimidazoles (26-31) have been prepared starting from 2-substituted 4-aminophenols (1-3) or 4-chloro-4'-hydroxy-3-nitrobenzophenone (5).The mechanism of formation of benzimidazol-2-one by the reaction of o-phenylenediamine with 1,3-dicarbethoxy-S-methylisothiourea in refluxing DMF is also discussed.A number of compounds have been tested for their antifilarial, antihookworm and cestodicidal activities against Litomosoides carnii, Ancylostoma ceylanicum and Hymenolepis nana respectively in rodents but none of them shows any significant activity.

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