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(4-Methoxy-phenyl)-[2-(3-methoxy-phenyl)-cyclopropyl]-methanone is a complex organic compound with the molecular formula C18H18O3. It features a methanone (ketone) functional group, with a 4-methoxy-phenyl group attached to the carbonyl carbon. The other part of the molecule consists of a cyclopropyl ring, which is substituted at the 2-position with a 3-methoxy-phenyl group. (4-Methoxy-phenyl)-[2-(3-methoxy-phenyl)-cyclopropyl]-methanone is characterized by its aromatic rings, which are electron-rich due to the presence of methoxy groups, and the cyclopropyl ring, which introduces a unique three-membered carbon cycle. The compound's structure and properties make it a potential candidate for various applications in the fields of pharmaceuticals, materials science, and organic chemistry, particularly in the synthesis of complex molecules and the study of ring strain effects.

74973-35-6

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74973-35-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74973-35-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,7 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74973-35:
(7*7)+(6*4)+(5*9)+(4*7)+(3*3)+(2*3)+(1*5)=166
166 % 10 = 6
So 74973-35-6 is a valid CAS Registry Number.

74973-35-6Relevant academic research and scientific papers

Reactions of Aryl Cyclopropyl Ketones. A New Synthesis of Aryl Tetralones

Murphy, William S.,Wattanasin, Sompong

, p. 2920 - 2926 (2007/10/02)

Aryl cyclopropyl ketones (2) cyclise to 1-tetralones (3) in the presence of a variety of acid catalysts under mild conditions.Open-chain carbinols (4) are also formed.The ratio of (3) to (4) is dependent on the aryl ring substituents.A cationic mechanism is proposed.Cyclopropyl ketones (1) do not react.Stereoelectronic factors involved in the reactivity of the rigig cyclopropyl ketone (12) are discussed.The reactions of selected phenolic cyclopropyl ketones have been investigated as anionic counterparts to the acid-catalysed reactions.No reaction is observed.

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