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2,2,6,6-Tetraphenylcyclohexanone is an organic compound characterized by its unique molecular structure, which consists of a cyclohexanone ring with four phenyl groups attached to the carbon atoms at positions 2, 2, 6, and 6. 2,2,6,6-tetraphenylcyclohexanone is known for its high symmetry and rigidity, which can influence its physical and chemical properties. It is often used in the synthesis of various organic compounds and as a building block in the creation of more complex molecules. Due to its stability and the presence of aromatic rings, it can also be found in research related to materials science and pharmaceuticals. The compound's molecular formula is C38H30O, and it is typically synthesized through a series of chemical reactions involving cyclohexanone and phenyl groups.

83576-30-1

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83576-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83576-30-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,7 and 6 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 83576-30:
(7*8)+(6*3)+(5*5)+(4*7)+(3*6)+(2*3)+(1*0)=151
151 % 10 = 1
So 83576-30-1 is a valid CAS Registry Number.

83576-30-1Relevant academic research and scientific papers

Pentavalent Organobismuth Reagents. Part 3. Phenylation of Enols and of Enolate and other Anions

Barton, Derek H. R.,Blazejewski, Jean-Claude,Charpiot, Brigitte,Finet, Jean-Pierre,Motherwell, William B.,et al.

, p. 2667 - 2676 (2007/10/02)

The phenylation of enols and of enolate anions of ketones, β-diketones and keto esters has been studied using a range of Bi reagents.Under basic conditions C-phenylation is observed and, even hindered, perphenylated compounds are easily synthesized.Under neutral and acidic conditions ordinary ketones do not react and enolic systems give O-phenylation.A number of other anions have been phenylated under basic conditions, including the key compound indole wich mainly gave 3-C-phenylation.All these reactions can be supposed to have one of two alternative mechanisms, which parallel the two mechanisms proposed for the phenylation of phenols.

Synthesis and X-Ray Crystal Structures of some Hindered Polyphenylated Ketones

Barton, Derek H. R.,Papoula, Teresa Barros,Guilhem, Jean,Motherwell, William B.,Pascard, Claudine,Dau, Elise Tran Huu

, p. 732 - 734 (2007/10/02)

The synthesis, properties, and X-ray structures of two highly hindered polyphenylated ketones, 2,2,6,6-tetraphenylcyclohexanone and pentaphenylacetone, are described, both being obtained using bismuth(V) chemistry.

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