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2‐(2‐(4‐(dimethylamino)phenyl)‐4,5‐diphenyl‐1H‐imidazol‐1‐yl)acetohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

255065-88-4

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255065-88-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 255065-88-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,0,6 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 255065-88:
(8*2)+(7*5)+(6*5)+(5*0)+(4*6)+(3*5)+(2*8)+(1*8)=144
144 % 10 = 4
So 255065-88-4 is a valid CAS Registry Number.

255065-88-4Relevant academic research and scientific papers

Synthesis of imidazole derivatives: Ester and hydrazide compounds with antioxidant activity using ionic liquid as an efficient catalyst

Abdelhamid, Antar A.,Salah, Hanan A.,Marzouk, Adel A.

, p. 676 - 685 (2019/11/14)

The pyrrolidinium hydrogen sulfate (PHS) was used as an excellent ionic liquid catalyst for the preparation of many imidazoles moiety, which have biologically application via one-pot multicomponent reaction. Imidazoles were afforded through the reaction o

Substituted imidazole derivatives as novel cardiovascular agents

Malhotra, Vineet,Pathak, Seema R.,Nath, Rajendra,Mukherjee, Devashish,Shanker

, p. 936 - 939 (2011/03/20)

A series of novel substituted imidazole derivatives were synthesized and have been screened in vivo for their hypotensive and acute toxicity activities. Out of seventeen compounds eight compounds (2b, 2c, 3b, 3c, 3f, 4a, 4b and 4c) have shown good hypoten

Cardiovascular effects of novel imidazoline congeners

Shukla,Bhalla,Misra,Mukerjee,Saxsena,Sinha,Shanker

, p. 229 - 232 (2007/10/03)

2-Aryl-4,5-bis(diphenyl)-1-(N-acetyl hydrazide)-1,3-imidazoline (IIb1- 4) was prepared by the reaction of ethyl chloro acetate and hydrazine hydrate with 2-Aryl-4,5-bis (diphenyl) - 1H - imidazoline (I a1-4), which on further substitution with aryl/heterocyclyl aldheyde gave 2-Aryl-4,5-his (diphenyl)- 1-(4-substituted hydrazone) -1,3 - imidazoline (III Ca-1). This was again cyclised to oxadiazole in the presence of ferric chloride and glacial acetic acid yielded 2-Aryl-4,5-bis(diphenyl)-1-(2-substituted-1,3,4-oxadizole)-1,3- imidazoline (IV da-i). These compounds were screened for hypotensive activity and an attempt were made to get the site of action of these compounds.

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