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9-Phenyl-9-phosphabicyclo[4.2.1]nonatriene oxide, also known as 9-phenyl-9-phosphonia-4,5,6,7-tetrahydro-1H-fluorene oxide, is a complex organic compound with the molecular formula C15H15OP. It is a phosphorus-containing derivative of the bicyclic nonatriene oxide structure, featuring a phenyl group attached to the phosphorus atom. 9-phenyl-9-phosphabicyclo[4.2.1]nonatriene oxide is of interest in the field of organic chemistry, particularly in the study of phosphorus-containing heterocycles and their potential applications in materials science and pharmaceuticals. It is synthesized through various chemical reactions and can be used as a building block for more complex molecules or as a reagent in organic synthesis. The compound's properties, such as its reactivity and stability, are influenced by the presence of the phosphorus atom and the aromatic phenyl group, making it a subject of research for its unique chemical behavior and potential uses.

7289-62-5

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7289-62-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7289-62-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,8 and 9 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7289-62:
(6*7)+(5*2)+(4*8)+(3*9)+(2*6)+(1*2)=125
125 % 10 = 5
So 7289-62-5 is a valid CAS Registry Number.

7289-62-5Relevant academic research and scientific papers

Catalytic wittig reactions of semi- and nonstabilized ylides enabled by ylide tuning

Coyle, Emma E.,Doonan, Bryan J.,Holohan, Andrew J.,Walsh, Killian A.,Lavigne, Florie,Krenske, Elizabeth H.,O'Brien, Christopher J.

, p. 12907 - 12911 (2014)

The first examples of catalytic Wittig reactions with semistabilized and nonstabilized ylides are reported. These reactions were enabled by utilization of a masked base, sodium tert-butyl carbonate, and/or ylide tuning. The acidity of the ylide-forming proton was tuned by varying the electron density at the phosphorus center in the precatalyst, thus facilitating the use of relatively mild bases. Steric modification of the precatalyst structure resulted in significant enhancement of E selectivity up to >95:5, E/Z. Time for a tune up: Catalytic Wittig reactions with semi- and nonstabilized ylides were enabled by use of a masked base (NaOCO2tBu) and/or ylide tuning. The acidity of the ylide-forming proton was tuned by varying the electron density at the P center in the precatalyst, thus facilitating the use of relatively mild bases. Steric modification of the precatalyst structure resulted in significant enhancement of E selectivity.

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