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Ethanedial, mono[(4-nitrophenyl)hydrazone], also known as glyoxal mono(4-nitrophenylhydrazone), is a chemical compound with the molecular formula C8H8N4O3. It is a derivative of glyoxal, an organic compound consisting of two carbon atoms double-bonded to each other, with one of the carbonyl groups (C=O) replaced by a 4-nitrophenylhydrazone group. Ethanedial, mono[(4-nitrophenyl)hydrazone] is often used as a reagent in organic synthesis and analytical chemistry, particularly for the detection and determination of aldehydes and ketones. The 4-nitrophenylhydrazone group is known for its ability to form colored complexes with carbonyl compounds, which can be used for qualitative and quantitative analysis. The compound is typically synthesized by reacting glyoxal with 4-nitrophenylhydrazine, and it is characterized by its yellow crystalline appearance.

3078-12-4

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3078-12-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3078-12-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,7 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3078-12:
(6*3)+(5*0)+(4*7)+(3*8)+(2*1)+(1*2)=74
74 % 10 = 4
So 3078-12-4 is a valid CAS Registry Number.

3078-12-4Relevant academic research and scientific papers

Iridium(III)-Catalyzed Direct C-H Sulfonamidation of 2-Aryl-1,2,3-triazole N-Oxides with Sulfonyl Azides

Zhu, Bingfeng,Cui, Xiuling,Pi, Chao,Chen, Dong,Wu, Yangjie

supporting information, p. 326 - 332 (2016/02/14)

We have developed a method for the direct sulfonamidation of 2-aryl-1,2,3-triazole N-oxides using sulfonyl azides as the amino source to release molecular nitrogen as the sole by-product. This protocol exhibits excellent functional group tolerance and proceeds efficiently under external oxidant-free conditions. Various 2-(2-sulfonamidoaryl)-1,2,3-triazoles were prepared in up to 97% yields for 25 examples with excellent regioselectivity.

OXYGENATION OF 4-NITROPHENYLHYDRAZONES α,β-ENONES WITH Co(SALPR)

Nishinaga, Akira,Yamazaki, Shigekazu,Matsuura, Teruo

, p. 1729 - 1732 (2007/10/02)

Oxygenation of 4-nitrophenylhydrazones of α,β-enones with Co(Salpr), a five coordinated cobalt(II) Schiff base complex, results in the oxidative cleavage of the double bond in the substrate.A proposed mechanism involves the decomposition of peroxidic inte

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