51674-05-6 Usage
Uses
Used in Pharmaceutical Industry:
(2-AMINOPHENYL)(PHENYL)METHANONE OXIME is used as a building block for the synthesis of pharmaceutical compounds due to its potential biological activity and versatility in chemical reactions.
Used in Dye Production:
(2-AMINOPHENYL)(PHENYL)METHANONE OXIME is used as a precursor in the production of dyes, leveraging its chemical properties to create a wide range of colorants for various applications.
Used in Agrochemical Industry:
(2-AMINOPHENYL)(PHENYL)METHANONE OXIME is used as a key intermediate in the synthesis of agrochemicals, contributing to the development of effective and environmentally friendly products for agricultural use.
Used in Industrial Chemicals Production:
(2-AMINOPHENYL)(PHENYL)METHANONE OXIME is used as a reagent in the production of various industrial chemicals, taking advantage of its properties to facilitate chemical reactions and synthesize desired products.
Used in Organic Synthesis:
(2-AMINOPHENYL)(PHENYL)METHANONE OXIME is used as a reagent in organic synthesis, enabling the formation of complex organic molecules and contributing to the advancement of chemical research and development.
Used in Coordination Chemistry:
(2-AMINOPHENYL)(PHENYL)METHANONE OXIME is used as a ligand in coordination chemistry, playing a crucial role in the formation of coordination compounds and expanding the understanding of metal-ligand interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 51674-05-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,7 and 4 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51674-05:
(7*5)+(6*1)+(5*6)+(4*7)+(3*4)+(2*0)+(1*5)=116
116 % 10 = 6
So 51674-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H12N2O/c14-12-9-5-4-8-11(12)13(15-16)10-6-2-1-3-7-10/h1-9,16H,14H2/b15-13+
51674-05-6Relevant academic research and scientific papers
Eco-friendly H2O2 oxidation of 1,2-dihydroquinazoline-3-oxides to quinazoline-3-oxides
Samandram, Rashinikumar,?etin Koruk?u, Meliha,Co?kun, Necdet
supporting information, p. 2349 - 2356 (2021/06/14)
2-Aminobenzaldehyde, 1-(2-aminophenyl)ethanone, and 2-aminophenyl phenyl methanone oximes 1 were reacted with aromatic aldehydes to give the corresponding 1,2-dihydroquinazoline-3-oxides 2. The latter were converted in high yields to a series of quinazoli
An efficient synthesis of quinazolines: a theoretical and experimental study on the photochemistry of oxime derivatives
Alonso, Rafael,Caballero, Alegría,Campos, Pedro J.,Sampedro, Diego,Rodríguez, Miguel A.
experimental part, p. 4469 - 4473 (2010/07/08)
A new photochemical method for the preparation of quinazolines (2) through irradiation of [2-(methyleneamino)phenyl]methanone oximes (1) is reported. The photoreaction has been studied in depth by experimental, theoretical and photochemical methods. A six-electron electrocyclic ring closure mechanism, followed by water loss, is proposed and rationalized to explain the formation of quinazolines (2).
Intramolecular Cyclization of Iminoxyl Radicals
Atmaram, Shiravanate,Forrester, Alexander R.,Gill, Melvyn,Napier, Russell J.,Thomson, Ronald H.
, p. 641 - 648 (2007/10/02)
Iminyl radicals, generated by oxidation of the corresponding O-carboxymethoximes with persulfate, do not cyclise onto an ajacent azo group but the structurally related iminoxyls cyclise to give indazoles.ESR evidence is presented for the intramolecular ad
