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9-(4-fluorobenzyl)-9H-fluoren-9-ol is a synthetic organic compound characterized by its unique molecular structure. It features a fluoren-9-ol core, which is a derivative of fluorene, a polycyclic aromatic hydrocarbon. The molecule is further distinguished by the presence of a 4-fluorobenzyl group attached to the fluoren-9-ol scaffold. This fluorinated benzyl group introduces a fluorine atom into the molecule, which can significantly alter its chemical properties, such as reactivity, lipophilicity, and electronic characteristics. The compound is of interest in various fields, including materials science, medicinal chemistry, and as a potential intermediate in the synthesis of more complex molecules. Its specific applications may range from the development of new pharmaceuticals to the creation of advanced materials with unique properties.

379-81-7

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379-81-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 379-81-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 379-81:
(5*3)+(4*7)+(3*9)+(2*8)+(1*1)=87
87 % 10 = 7
So 379-81-7 is a valid CAS Registry Number.

379-81-7Relevant academic research and scientific papers

Ligand-Free Ru-Catalyzed Direct sp3 C-H Alkylation of Fluorene Using Alcohols

Shaikh, Moseen A.,Agalave, Sandip G.,Ubale, Akash S.,Gnanaprakasam, Boopathy

, p. 2277 - 2290 (2020)

The sp3 C-H alkylation of 9H-fluorene using alcohol and a Ru catalyst via the borrowing hydrogen concept has been described. This reaction was catalyzed by the [Ru(p-cymene)Cl2]2 complex (3 mol %) and exhibited a broad reaction scope with different alcohols, allowing primary and secondary alcohols to be employed as nonhazardous and greener alkylating agents with the formation of environmentally benign water as a byproduct. A variety of 9H-fluorene underwent selective and exclusive mono-C9-alkylation with primary alcohols in good to excellent isolated yield (26 examples, 50-92% yield), whereas this reaction with secondary alcohols in the absence of any external oxidants furnished the tetrasubstituted alkene as the major product. Furthermore, a base-mediated C-H hydroxylation of the synthesized 9H-fluorene derivatives afforded 9H-hydroxy-functionalized quaternary fluorene derivatives in excellent yield.

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