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Pyridine, 2-(1-phenylhydrazino)-, also known as 2-(1-phenylhydrazino)pyridine, is an organic compound with the chemical formula C11H10N2. It is a derivative of pyridine, a heterocyclic aromatic compound with a nitrogen atom in the ring structure. This particular compound features a phenyl group (C6H5) attached to the hydrazine (NH-NH2) moiety, which is further connected to the pyridine ring at the 2-position. It is a colorless to pale yellow solid and is soluble in common organic solvents. 2-(1-phenylhydrazino)pyridine is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain anti-inflammatory and antipyretic drugs. Due to its reactivity, it is important to handle Pyridine, 2-(1-phenylhydrazino)- with care, following proper safety protocols.

4231-72-5

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4231-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4231-72-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,3 and 1 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4231-72:
(6*4)+(5*2)+(4*3)+(3*1)+(2*7)+(1*2)=65
65 % 10 = 5
So 4231-72-5 is a valid CAS Registry Number.

4231-72-5Relevant academic research and scientific papers

Heteroarylation method of amine

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Paragraph 0060-0072; 0079, (2021/02/24)

The invention discloses a heteroarylation method of amine, and the method comprises the following steps of: mixing an amine compound, heteroaromatic hydrocarbon, a photocatalyst and an organic solventto obtain a solution A; and in an inert gas atmosphere, irradiating the solution A with visible light, and carrying out reaction to obtain a heteroarylated product of amine. According to the method,under mild conditions, free radical coupling of amine compounds and heteroaromatic compounds is efficiently achieved through visible light irradiation, and various heteroarylamines are synthesized. The method has good functional group compatibility and high regioselectivity, can be further applied to later modification of bioactive molecules, and shows a good industrial application prospect.

An easy route to N,N-diarylhydrazines by Cu-catalyzed arylation of pyridine-2-carbaldehyde hydrazones with aryl halides

Wu, Wei,Li, Xin-Le,Fan, Xin-Heng,Yang, Lian-Ming

, p. 862 - 867 (2013/03/28)

A copper-catalyzed C-N coupling reaction is described for the preparation of pyridine-2-carbaldehyde N,N-diarylhydrazones by the arylation of N-mono- or -non-substituted hydrazones with aryl bromides/iodides, and the subsequent conversion of the hydrazones into N,N-diarylhydrazines by a transimination process with an aqueous solution of H2NNH2. The reaction features the use of CuI as the catalyst without the need for external ligands. This methodology provides a convenient alternative to the synthesis of structurally diverse N,N-diarylhydrazines from simple, easily accessible precursors. Copyright

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