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

10432-55-0

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10432-55-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10432-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,3 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10432-55:
(7*1)+(6*0)+(5*4)+(4*3)+(3*2)+(2*5)+(1*5)=60
60 % 10 = 0
So 10432-55-0 is a valid CAS Registry Number.

10432-55-0Downstream Products

10432-55-0Relevant academic research and scientific papers

Synthesis of dimethyl glutarate from cyclobutanone and dimethyl carbonate over solid base catalysts

Zhi, Chen,Dudu, Wu

experimental part, p. 1834 - 1838 (2012/07/31)

A facile route for the synthesis of dimethyl glutarate (DMG) from cyclobutanone and dimethyl carbonate (DMC) in the presence of solid base catalysts has been developed. It was found that the intermediate carbomethoxycyclobutanone (CMCB) was produced from cyclobutanone with DMC in the first step, and then CMCB was further converted to DMG by reacting with a methoxide group. The role of the basic catalysts can be mainly ascribed to the activation of cyclobutanone via the abstraction of a proton in the α-position by base sites, and solid bases with moderate strength, such as MgO, favor the formation of DMG.

Reactions of alkali metal anions. XV. Reaction of ketones with alkali metal anions

Jedlinski,Misioiek,Giowkowski,Janeczek,Wolinska

, p. 3547 - 3558 (2007/10/02)

The potassium anions were found to react with ketones to39 yield both alcoholates and enolates. On the basis of the ESR and K NMR measurements the mechanism of this reaction is proposed. According to the proposed mechanism in the first step a ketyl radical is formed which after disproportionation yields an enolate and an alcoholate but only in the case of ketones having hydrogen atom in α-position in respect to carbonyl group.

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