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1,2-Diphenyl-3-methylcyclopropene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51425-87-7

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51425-87-7 Usage

Type of compound

Cyclopropene derivative

Structural features

Contains two phenyl groups
Contains a methyl group
Attached to the cyclopropene ring

Reactivity

Highly reactive in certain chemical reactions due to its three-membered ring structure

Applications

Organic synthesis
Chemical research
Building block for creating other organic compounds

Potential uses

Pharmaceuticals
Agrochemicals
Materials science

Unique properties

Versatile reactivity and structural features

Check Digit Verification of cas no

The CAS Registry Mumber 51425-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,2 and 5 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51425-87:
(7*5)+(6*1)+(5*4)+(4*2)+(3*5)+(2*8)+(1*7)=107
107 % 10 = 7
So 51425-87-7 is a valid CAS Registry Number.

51425-87-7Relevant academic research and scientific papers

The reaction of benzotrihalides and benzal halides with magnesium. Synthetic and mechanistic studies

Ashby, E. C.,Al-Fekri, Dheya M.

, p. 275 - 292 (2007/10/02)

The benzotrihalides (PhCX3) where X = Cl, Br, and F were allowed to react with magnesium in THF at room temperature.When the halide was chloride or bromide, the trihalide gave diphenylacetylene in high yield in addition to several minor products which were identified.No reaction was observed when the halide was fluoride.When the corresponding dichloride was allowed to react with magnesium in THF, stilbene was formed as the major product.The possible mechanisms for these reactions are discussed.

Single-Electron-Transfer Pathway in the Coupling of Cyclopropenyl Cations with Organometallic Reagents

Padwa, Albert,Goldstein, Steven I.,Rosenthal, Robert J.

, p. 3278 - 3285 (2007/10/02)

Treatment of diphenylmethylcyclopropenylium perchlorate with various Grignard reagents produced substituted cyclopropenes in excellent yield.Alkyl and vinylic Grignard reagents react at the methylated carbon atom.The substantial increase in formation of t

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