51674-05-6 Usage
General Description
(2-Aminophenyl)(phenyl)methanone oxime is a chemical compound with the molecular formula C13H11N3O. It is a white crystalline solid that is commonly used as a reagent in organic synthesis and as a ligand in coordination chemistry. (2-AMINOPHENYL)(PHENYL)METHANONE OXIME has potential applications in pharmaceuticals and can also be used in the production of dyes, agrochemicals, and other industrial chemicals. Its properties and structure make it useful in various chemical reactions and as a building block in the synthesis of more complex organic molecules. Additionally, it may also have potential biological activity and could be of interest as a lead compound for drug discovery and development.
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 articles and documents
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
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
