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(4-Methylphenyl)(c-2,t-3-diphenylcycloprop-r-1-yl)methanon is a complex organic compound with the molecular formula C27H23. It is characterized by a unique structure that includes a 4-methylphenyl group attached to a cyclopropane ring, which is further substituted with two phenyl groups. (4-Methylphenyl)(c-2,t-3-diphenylcycloprop-r-1-yl)methanon is of interest in organic chemistry due to its potential applications in the synthesis of pharmaceuticals and other specialty chemicals. The cyclopropane ring, a three-carbon ring, is a strained system that can participate in various chemical reactions, making (4-Methylphenyl)(c-2,t-3-diphenylcycloprop-r-1-yl)methanon a valuable building block for more complex molecules. Its synthesis and reactivity are areas of ongoing research, as the properties of such strained rings can lead to the development of new drugs and materials.

86118-53-8

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86118-53-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86118-53-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,1 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 86118-53:
(7*8)+(6*6)+(5*1)+(4*1)+(3*8)+(2*5)+(1*3)=138
138 % 10 = 8
So 86118-53-8 is a valid CAS Registry Number.

86118-53-8Downstream Products

86118-53-8Relevant academic research and scientific papers

Generation of Diastereomeric Cyclopropanes from Benzylidenesulfuranes and Chalcones

Stahl, Ingfried,Schomburg, Sabine,Kalinowski, Hans Otto

, p. 2247 - 2260 (2007/10/02)

The reaction of the benzylidenesulfuranes 2, available by deprotonation of the benzylsulfonium bromides 1, with chalcones 3, which are substituted in the aroyl part, leads to the stereoisomeric cyclopropanes 4 and 5.The stereochemistry of 4 and 5 is elucidated by spectroscopy.A carbenic mechanism of formation of 4 and 5 is excluded experimentally.

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