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2-(N'-benzylidenehydrazino)-3-phenylquinoxaline is a complex organic compound with the molecular formula C21H16N4. It is characterized by a quinoxaline ring system, which is a fused bicyclic structure consisting of a pyrazine and a benzene ring. The molecule features a hydrazino group attached to the 2-position of the quinoxaline, and a benzylidene group that forms a double bond with the hydrazino nitrogen, creating an extended conjugated system. Additionally, a phenyl group is attached to the 3-position of the quinoxaline ring. 2-(N'-benzylidenehydrazino)-3-phenylquinoxaline is of interest in the field of heterocyclic chemistry and may have potential applications in pharmaceuticals or materials science due to its unique structure and electronic properties.

1049-25-8

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1049-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1049-25-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,4 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1049-25:
(6*1)+(5*0)+(4*4)+(3*9)+(2*2)+(1*5)=58
58 % 10 = 8
So 1049-25-8 is a valid CAS Registry Number.

1049-25-8Relevant academic research and scientific papers

Copper(II) chloride mediated synthesis and DNA photocleavage activity of 1-aryl/heteroaryl-4-substituted-1,2,4-triazolo[4,3-a]quinoxalines

Aggarwal, Ranjana,Sumran, Garima,Kumar, Virender,Mittal, Ashwani

experimental part, p. 6083 - 6088 (2012/01/03)

A new class of photonucleases, 1-aryl/heteroaryl-4-substituted-1,2,4- triazolo[4,3-a]quinoxalines (4) was synthesized in a facile and efficient manner via copper(II) chloride mediated oxidative intramolecular cyclization of 2-(arylidenehydrazino)-3-substi

Quinoxaline derivatives part II: Synthesis and antimicrobial testing of 1,2,4-triazolo[4,3-a]quinoxalines, 1,2,4-triazino[4,3-a]quinoxalines and 2- pyrazolylquinoxalines

El-Hawash,Habib,Fanaki

, p. 808 - 813 (2007/10/03)

Three main classes of quinoxaline derivatives have been synthesized. The first class comprises the synthesis of three novel series of 1,2,4- triazolo[4,3-a]quinoxalines; namely 1-substituted-1,2,4-triazolo[4,3- a]quinoxalines 3a-f, 1-substituted aminomethyl-1,2,4-triazolo[4,3- a]quinoxalines 14a-d and 1-cyano or ethoxycarbonylmethyl-1,2,4- triazolo[4,3a]quinoxalines 6, 12. The second class involves the synthesis of 2-substituted-1H-1,2,4-triazino[4,3-a]quinoxalines 4a-d. The third class deals with the synthesis of a variety of 2-pyrazolylquinoxalines, namely 2- (5-amino-3-arylpyrazol-1-yl)-3-phenylquinoxalines 5a-d, 2-[5-hydroxy-3- phenyl-4-(4-substituted sulfamoylphenyl)azopyrazol-1-yl]-3-phenylquinoxalines 15a, b, and 2-(5-hydroxy-4-nitroso-3-phenylpyrazol-1-yl)-3-phenylquinoxaline (16). The prepared compounds were tested in vitro for their antimicrobial activity. Compounds 13 and 14b exhibited promising antifungal activity against C. albicans (MIC 25, 50 μ/ml respectively). Compound 13 was as active as the antibiotic nystatin.

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