4127-56-4 Usage
Uses
Used in Pharmaceutical Industry:
Ethanone, 1-(2-amino-6-methylphenyl)(9CI) is utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Industry:
In the agrochemical sector, Ethanone, 1-(2-amino-6-methylphenyl)(9CI) serves as a key intermediate in the production of agrochemicals, contributing to the creation of effective solutions for agricultural applications.
Used in Organic Compounds Synthesis:
Ethanone, 1-(2-amino-6-methylphenyl)(9CI) is also employed in the synthesis of other organic compounds, showcasing its versatility and potential for diverse applications across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 4127-56-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,1,2 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4127-56:
(6*4)+(5*1)+(4*2)+(3*7)+(2*5)+(1*6)=74
74 % 10 = 4
So 4127-56-4 is a valid CAS Registry Number.
4127-56-4Relevant academic research and scientific papers
Modification of Photochemical Reactivity by Cyclodextrin Complexation: Product Selectivity in Photo-Fries Rearrangement
Syamala, M. S.,Rao, B. Nageswer,Ramamurthy, V.
, p. 7234 - 7242 (2007/10/02)
Cyclodextrin encapsulation, both in the solid state and in aqueous solution brings about a remarkable regulation of the photo-Fries rearrangement of phenyl esters and anilides.In comparison to the non-selective mixture of ortho and para-rearranged isomers along with the deacylated product obtained in organic solvents, the solid β-cyclodextrin complexes of unsubstituted esters and anilides show a remarkable 'ortho-selectivity'.An impressive 'regio-selectivity' among the two ortho-rearranged isomers is observed for meta-substituted esters and anilides upon irradiation as β-cyclodextrin complexes.Specific orientations of the unsubstituted and meta-substituted esters and anilides in the β-cyclodextrin cavity are suggested to be responsible for the observed selectivity.
