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51425-87-7

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51425-87-7 Usage

General Description

1,2-Diphenyl-3-methylcyclopropene is a chemical compound with the molecular formula C17H16. It is a cyclopropene derivative that contains two phenyl groups and a methyl group attached to the cyclopropene ring. 1,2-Diphenyl-3-methylcyclopropene is commonly used in organic synthesis and chemical research as a building block for creating other organic compounds. It is known for its unique properties, including its three-membered ring structure, which can make it highly reactive in certain chemical reactions. 1,2-Diphenyl-3-methylcyclopropene has potential applications in pharmaceuticals, agrochemicals, and materials science due to its 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 articles and documents

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.

Preparation of chlorophenyldiazirine and thermal generation of chlorophenyl carbene: 1,2-Diphenyl-3- methylcyclopropene

Padwa, Albert,Pulwer, Mitchell J.,Blacklock, Thomas J.

, p. 53 - 53 (2017/05/17)

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