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α,α-Diphenyl-4-ethylacetophenone is an organic compound with the chemical formula C20H20O. It is a derivative of acetophenone, featuring two phenyl groups attached to the alpha carbon and an ethyl group on the para position. This colorless to pale yellow crystalline solid is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity, it is often employed in the synthesis of various chemical compounds, particularly those involving the formation of carbon-carbon bonds. The compound is also known for its potential applications in the field of materials science, such as in the development of new polymers and other advanced materials.

75187-48-3

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75187-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75187-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,1,8 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75187-48:
(7*7)+(6*5)+(5*1)+(4*8)+(3*7)+(2*4)+(1*8)=153
153 % 10 = 3
So 75187-48-3 is a valid CAS Registry Number.

75187-48-3Downstream Products

75187-48-3Relevant academic research and scientific papers

Acylation of aromatic substrates with ketenes. An example of vinyl oxocation reactivity.

Fountain, K.R.,Heinze, Pamela,Sherwood, Mark,Maddex, Dave,Gerhardt, Greg

, p. 1198 - 1205 (2007/10/02)

Acylations of aromatic substrates with ketenes involve the reactivity of species similar to vinyl cations.Resonance stabilization of ketene-aluminum chloride complexes seems to make these complexes less reactive than corresponding vinyl cations.The kinetic isotope effect of the reaction with dimethylketene and benzene is 1.06, compatible with vinylcation cases, but not with acylation with CH3COBF4 types of electrophiles.Substrate specificity was determined from k (toluene)/k (benzene) values.It was 47.2 for dimethylketene and 173.7 for diphenylketene.The diphenylketene-aluminum chloride complex could be isolated.

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