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(E)-1,7-diphenyl-6-hepten-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28069-38-7

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28069-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 28069-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,0,6 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 28069-38:
(7*2)+(6*8)+(5*0)+(4*6)+(3*9)+(2*3)+(1*8)=127
127 % 10 = 7
So 28069-38-7 is a valid CAS Registry Number.

28069-38-7Downstream Products

28069-38-7Relevant academic research and scientific papers

Nickel-catalyzed Suzuki Coupling of Cycloalkyl Silyl Peroxides with Boronic Acids

Chen, Lei,Duan, Xin-Hua,Guo, Li-Na,Xu, Pengfei,Yang, Jun-Cheng,Zhang, Jun-Jie

, p. 7515 - 7525 (2020/06/27)

A nickel-catalyzed Suzuki alkyl-aryl coupling of cycloalkyl silyl peroxides with boronic acids is reported. The primary and secondary ketoalkyl electrophiles generated through C-C bond cleavage were amenable, providing rapid access to a variety of distal arylated alkyl ketones. A radical pathway is proposed for this reaction.

Iron-Catalyzed Decarboxylative Olefination of Unstrained Carbon-Carbon Bonds Relying on Alkoxyl Radical Induced Cascade

Gao, Pin,Wu, Hao,Yang, Jun-Cheng,Guo, Li-Na

, p. 7104 - 7108 (2019/09/30)

An iron-catalyzed decarboxylative olefination of unstrained carbon-carbon bonds via alkoxyl radical induced C-C bond cleavage is presented. This protocol features mild conditions (room temperature, redox-neutral), good substrate scope and functional group

Synthesis of hexahydrocyclopenta[c]furans by an intramolecular iron-catalyzed ring expansion reaction

Hilt, Gerhard,Bolze, Patrick,Heitbaum, Maja,Hasse, Katrin,Harms, Klaus,Massa, Werner

, p. 2018 - 2026 (2008/09/17)

The intramolecular iron-catalyzed ring expansion reaction of epoxyalkenes was investigated with a preformed iron(salen) [Fe(Salen)] complex. The formal insertion of the alkene into the epoxide generated hexahydrocyclopenta[c]furan derivatives in moderate to good yields and diastereoselectivities depending on other functional groups present in the starting materials. In addition, oxygen-tethered epoxyalkenes were used for the synthesis of lignan isomers. The scope and limitations of the Fe (Salen)-catalyzed process of the reaction are discussed.

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