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Ethyl glyoxalate p-nitrophenylhydrazone is a chemical compound with the molecular formula C10H12N4O3. It is derived from the reaction of ethyl glyoxalate with p-nitrophenylhydrazine, resulting in the formation of a hydrazone derivative. ethyl glyoxalate p-nitrophenylhydrazone is characterized by its yellow crystalline appearance and is soluble in common organic solvents such as ethanol and acetone. Ethyl glyoxalate p-nitrophenylhydrazone is primarily used as an analytical reagent in the detection and quantification of aldehydes and ketones due to its ability to form colored complexes with these compounds. Its chemical structure and properties make it a valuable tool in various research and industrial applications, particularly in the field of organic chemistry and chemical analysis.

5634-73-1

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5634-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5634-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,3 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5634-73:
(6*5)+(5*6)+(4*3)+(3*4)+(2*7)+(1*3)=101
101 % 10 = 1
So 5634-73-1 is a valid CAS Registry Number.

5634-73-1Relevant academic research and scientific papers

Silver(I)-Catalyzed Tandem Sigamatropic Rearrangement/1,3-H Shift/6π Aza-electrocyclization of N-Propargylic Hydrazones: A Mild Synthetic Route to 1,6-Dihydropyridazines

Ding, Zong-Cang,Ju, Lu-Chuan,Yang, Ying,An, Xiao-Ming,Zhou, Yun-Bing,Li, Ren-Hao,Tang, Hai-Tao,Ding, Cheng-Ke,Zhan, Zhuang-Ping

, p. 3936 - 3941 (2016/05/24)

A highly efficient AgOTf catalyzed [3,3] sigmatropic rearrangement/1,3-H shift/6' aza-electrocyclization cascade reaction of N-propargylic hydrazones has been developed. This method provides a new mild synthetic route to various polysubstituted 1,6-dihydr

Palladium and Copper Cocatalyzed Intermolecular Cyclization Reaction: Synthesis of 5-Aminopyrazole Derivatives

Ma, Chaowei,Wen, Ping,Li, Jihui,Han, Xu,Wu, Zhaoyang,Huang, Guosheng

supporting information, p. 1073 - 1077 (2016/04/09)

A novel and efficient palladium and copper co-catalyzed intermolecular cyclization of acetonitriles with hydrazones has been developed for the synthesis of 5-aminopyrazoles through C-C and C-N bond formation. The reaction has the advantages of easily avai

Vinylogous reactivity of enol diazoacetates with donor-acceptor substituted hydrazones. Synthesis of substituted pyrazole derivatives

Xu, Xinfang,Zavalij, Peter Y.,Hu, Wenhao,Doyle, Michael P.

, p. 1583 - 1588 (2013/03/28)

A regiospecific synthesis of multifunctional pyrazoleshas been developed from a cascade process triggered by Rh(II)-catalyzed dinitrogen extrusion from enol diazoacetates with vinylogous nucleophilic addition followed by Lewis acid catalyzed cyclization a

Pyrolysis of 3-hydroxy-2-arylhydrazonoalkanoic acid derivatives

Al-Awadi, Nouria A.,Ibrahim, Yehia A.,John, Elizabeth,Parveen, Aneesha

, p. 1298 - 1307 (2011/04/15)

1,2-Diaza-1,3-butadienes have been obtained from readily available 3-hydroxy-2-arylhydrazonopropanoates under various reaction conditions including pyrolysis, dehydration under Mitsunobu conditions or with acetic anhydride or acetic acid. According to their method of synthesis these 1,2-diaza-1,3- butadienes underwent subsequent reactions to give interesting products, and in the presence of proper dienophiles gave the corresponding cycloaddition products. Also, a new approach to pyrazole-3-carboxylic acid derivatives was discovered during an attempt to dehydrate 3-hydroxy-2-arylhydrazonobutanoic esters.

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