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2-(4-Biphenylyl)-2-phenyl-oxirane is a complex organic compound with the molecular formula C20H16O. It is a derivative of oxirane, also known as ethylene oxide, which features a three-membered ring containing one oxygen atom and two carbon atoms. In this specific compound, the oxirane ring is fused to a biphenyl group (two phenyl rings connected by a single bond) and a separate phenyl ring. The compound is characterized by its unique molecular structure, which may exhibit interesting chemical properties and potential applications in various fields, such as pharmaceuticals, materials science, and chemical research. Due to its complex structure, 2-(4-biphenylyl)-2-phenyl-oxirane may have unique reactivity and stability, making it a subject of interest for further study and potential development.

76952-48-2

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76952-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76952-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,9,5 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 76952-48:
(7*7)+(6*6)+(5*9)+(4*5)+(3*2)+(2*4)+(1*8)=172
172 % 10 = 2
So 76952-48-2 is a valid CAS Registry Number.

76952-48-2Relevant academic research and scientific papers

General theoretical treatments of solid-state photochemical rearrangements and a variety of contrasting crystal versus solution photochemistry

Zimmerman, Howard E.,Zhu, Zhaoning

, p. 5245 - 5262 (2007/10/02)

In continuing our investigations of control of excited state reactivity by inclusion in crystal lattices, we have encountered a variety of new examples of differing reactivity resulting from lattice restraints. Different theoretical treatments were tested

2-(4-Biphenylyl)-2-(halophenyl)-oxirane compounds

-

, (2008/06/13)

The invention relates to a process for the production of certain hydroxyethylazoles having antimycotic activity which comprises reacting selected phenyl-substituted oxiranes with azoles, preferably imidazoles or triazoles in the presence of an alkali meta

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