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Spiro[cyclohex[2]ene-1,9'-fluorene] is a complex organic compound with a unique molecular structure, consisting of a cyclohexene ring fused to a fluorene ring through a spiro linkage. This spiro compound is characterized by its rigid and planar structure, which arises from the fusion of the two aromatic rings. The compound is of interest in the field of organic chemistry, particularly in the study of aromatic systems and their potential applications in materials science, such as in the development of new polymers or as intermediates in the synthesis of more complex molecules. Its chemical properties and reactivity are influenced by the presence of the spiro junction, which can affect its electronic and steric characteristics.

6572-64-1

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6572-64-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6572-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6572-64:
(6*6)+(5*5)+(4*7)+(3*2)+(2*6)+(1*4)=111
111 % 10 = 1
So 6572-64-1 is a valid CAS Registry Number.

6572-64-1Downstream Products

6572-64-1Relevant academic research and scientific papers

Pd-catalyzed autotandem C-C/C-C bond-forming reactions with tosylhydrazones: Synthesis of spirocycles with extended π-conjugation

Barroso, Raquel,Valencia, Rocio A.,Cabal, Maria-Paz,Valdes, Carlos

, p. 2264 - 2267 (2014)

A new Pd-catalyzed autotandem process is presented by the reaction of tosylhydrazones of cyclic ketones and 2,2′-dibromobiphenyls and related systems. The process involves cross-coupling with tosylhydrazone followed by an intramolecular Heck reaction and gives rise to spirocyclic structures. Noteworthy, two C-CAr bonds are formed on the hydrazonic carbon during the process. Depending on the starting dibromide, an array of spirofluorenes, spirodibenzofluorenes, spiroacridines, and spiroanthracenes have been prepared. Thus, this methodology may be applied for the preparation of interesting structures useful in the development of optoelectronic materials.

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