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1-[4-(2-phenylhydrazinyl)phenyl]ethanone is a complex organic chemical compound with the molecular formula C15H14N2O. It is a derivative of acetophenone, featuring a phenyl group attached to the carbonyl group, and a phenylhydrazine moiety connected to the other phenyl ring. 1-[4-(2-phenylhydrazinyl)phenyl]ethanone is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through a condensation reaction involving acetophenone and 2-phenylhydrazine, and its properties, such as solubility and stability, can be influenced by the presence of functional groups and the overall molecular structure.

6311-55-3

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6311-55-3 Usage

Physical state

Yellow crystalline solid

Usage

Reagent in organic synthesis and pharmaceutical research

Potential applications

Dye intermediate, manufacturing of pharmaceuticals

Safety precautions

Harmful if ingested, inhaled, or comes into contact with skin or eyes

Handling

Handle with caution due to potential hazards

Check Digit Verification of cas no

The CAS Registry Mumber 6311-55-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6311-55:
(6*6)+(5*3)+(4*1)+(3*1)+(2*5)+(1*5)=73
73 % 10 = 3
So 6311-55-3 is a valid CAS Registry Number.

6311-55-3Relevant academic research and scientific papers

Convenient semihydrogenation of azoarenes to hydrazoarenes using H2

Sahoo, Manoj K.,Sivakumar, Ganesan,Jadhav, Sanjay,Shaikh, Samrin,Balaraman, Ekambaram

supporting information, p. 5289 - 5293 (2021/06/30)

The high atom-economical and eco-benign nature of hydrogenation reactions make them much more superior to conventional reduction and transfer hydrogenation. Herein, a convenient and highly selective hydrogenation reaction of azoarenes using molecular hydrogen to access diverse hydrazoarenes is reported. The present catalytic method is general and operationally simple, and it operates under exceedingly mild conditions (room temperature and 1 atm of hydrogen pressure). The reusability of catalysts used in this method is also successfully demonstrated.

Electrochemical dehydrogenation of hydrazines to azo compounds

Du, Ke-Si,Huang, Jing-Mei

supporting information, p. 1680 - 1685 (2019/04/08)

A strategy for the electrochemical dehydrogenation of hydrazine compounds is disclosed under ambient conditions. This protocol proceeded smoothly in ethanol by employing electrons as clean oxidants. Its synthetic value is well demonstrated by the highly efficient synthesis of symmetric and unsymmetric azo compounds. It is an environmentally friendly transformation and the present protocol was effective on a large scale.

The 4.4′-benzidine rearrangement of 4-alkyl substituted hydrazobenzenes

Bouillon, Marc E.,Meyer, Hartmut H.

, p. 3151 - 3161 (2016/05/24)

When treated with dilute inorganic acids N,N′-diarylhydrazines (hydrazobenzenes) with an alkyl substituent in the 4-position undergo [5,5]-sigmatropic rearrangement reactions to furnish 4-(4′-aminophenyl)-4-alkylcyclohexa-2,5-dienimines (ipso-benzidines) in moderate to excellent yields. Steric bulk of the 4-alkyl substituent in the starting material decreases the yield of the respective ipso-benzidine. Additional electron-donating alkyl substituents in the ortho- and/or meta-positions on both rings generally promote the reaction and consequently increase the yield of the 4.4′-benzidine rearrangement product. Described herein are our findings regarding the scope and limits of this unusual benzidine rearrangement.

Reactions of Azoarenes with Tributyltin Hydride

Alberti, Angelo,Bedogni, Nicola,Benaglia, Massimo,Leardini, Rino,Nanni, Daniele,et al.

, p. 607 - 613 (2007/10/02)

Tributyltin hydride when reacted with a series of substituted azoarenes afforded hydrazo compounds with high chemoselectivity and good to high yields.With ortho-substituted azoarenes, mixtures of hydrazo derivatives and N-heterocycles or cyclic products only were obtained.The kinetic law of the process was determined in the presence and in the absence of AIBN; with the radical initiator the reaction proceeds via a radical chain mechanism, whereas without AIBN the presence of stannyl free radicals could be discarded.The mechanism of the noninitiated reaction is discussed.EPR characterization of spin adducts obtained by reacting group IVB organometallic radicals with azo compounds is reported.

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