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2-cyclopropylcyclohexan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24892-74-8

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24892-74-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24892-74-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,8,9 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 24892-74:
(7*2)+(6*4)+(5*8)+(4*9)+(3*2)+(2*7)+(1*4)=138
138 % 10 = 8
So 24892-74-8 is a valid CAS Registry Number.

24892-74-8Relevant academic research and scientific papers

Synthesis of α,β-unsaturated carbonyl compounds via a visible-light-promoted organocatalytic aerobic oxidation

Zhang, Junlin,Wang, Leming,Liu, Qi,Yang, Zhen,Huang, Yong

supporting information, p. 11662 - 11664 (2013/12/04)

α,β-Unsaturated ketones and aldehydes have been synthesized from their corresponding silyl enol ethers in a straightforward protocol involving a visible-light promoted organocatalytic, aerobic oxidation reaction. A cheap organic dye was used catalytically in these reactions as the photosensitizer.

α-(Phenylthio)cyclopropylation of carbonyl compounds: Preparation of α-cyclopropyl ketones

Pohmakotr, Manat,Thisayukta, Jirakorn

, p. 6759 - 6762 (2007/10/03)

α-Chloro-α-(phenylthio)cyclopropane and α-acetoxy-α-(phenylthio)cyclopropane were found to react with the silyl enol ethers of some ketones in the presence of Lewis acid in dichloromethane to provide α-(phenylthio)cyclopropyl ketones, which were subjected to reduction with Ra-Ni to give the corresponding α-cyclopropyl ketones.

AN INTRAMOLECULAR ACYLATION OF OLEFINS DIRECTED BY TRIMETHYLSILYL GROUP. SYNTHESIS OF 2-CYCLOPROPYLCYCLOALKANONES

Hatanaka, Yasuo,Kuwajima, Isao

, p. 719 - 722 (2007/10/02)

An intramolecular acylation of ω-trimethylsilylacyl chlorides bearing C=C bonds at their appropriate positions takes place regioselectively to give the corresponding 2-cyclopropylcycloalkanones in the presence of TiCl4.

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