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4-aminophenylmesitylketone is an organic compound with the chemical formula C15H17NO. It is a derivative of phenylmesitylketone, featuring an amino group (-NH2) attached to the para position of the phenyl ring. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, particularly as a building block for the creation of complex molecules. The presence of the amino group allows for further chemical reactions, such as acylation or alkylation, which can lead to the formation of a wide range of compounds with different properties and uses. 4-aminophenylmesitylketone is also of interest in the field of materials science, where it may be used to develop new types of polymers or other advanced materials. Its unique structure and reactivity make it a valuable intermediate in organic synthesis.

1146-85-6

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1146-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146-85-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,4 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1146-85:
(6*1)+(5*1)+(4*4)+(3*6)+(2*8)+(1*5)=66
66 % 10 = 6
So 1146-85-6 is a valid CAS Registry Number.

1146-85-6Downstream Products

1146-85-6Relevant 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.

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