4127-56-4 Usage
General Description
Ethanone, 1-(2-amino-6-methylphenyl)- (9CI) is a chemical compound with the molecular formula C9H11NO. It is a derivative of ethanone that contains an amino group and a methyl group attached to a phenyl ring. Ethanone, 1-(2-amino-6-methylphenyl)- (9CI) is often used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is known for its pharmacological properties and potential therapeutic applications, although further research is needed to fully understand its bioactivity and mechanism of action. Overall, Ethanone, 1-(2-amino-6-methylphenyl)- (9CI) is a versatile chemical that holds promise for future developments in the field of medicinal chemistry.
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 articles and documents
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.
