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204699-72-9

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204699-72-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204699-72-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,6,9 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 204699-72:
(8*2)+(7*0)+(6*4)+(5*6)+(4*9)+(3*9)+(2*7)+(1*2)=149
149 % 10 = 9
So 204699-72-9 is a valid CAS Registry Number.

204699-72-9Upstream product

204699-72-9Downstream Products

204699-72-9Relevant academic research and scientific papers

Palladium-catalysed electrophilic aromatic C-H fluorination

Yamamoto, Kumiko,Li, Jiakun,Garber, Jeffrey A. O.,Rolfes, Julian D.,Boursalian, Gregory B.,Borghs, Jannik C.,Genicot, Christophe,Jacq, Jér?me,Van Gastel, Maurice,Neese, Frank,Ritter, Tobias

, p. 511 - 514 (2018)

Aryl fluorides are widely used in the pharmaceutical and agrochemical industries, and recent advances have enabled their synthesis through the conversion of various functional groups. However, there is a lack of general methods for direct aromatic carbon-hydrogen (C-H) fluorination. Conventional methods require the use of either strong fluorinating reagents, which are often unselective and difficult to handle, such as elemental fluorine, or less reactive reagents that attack only the most activated arenes, which reduces the substrate scope. A method for the direct fluorination of aromatic C-H bonds could facilitate access to fluorinated derivatives of functional molecules that would otherwise be difficult to produce. For example, drug candidates with improved properties, such as increased metabolic stability or better blood-brain-barrier penetration, may become available. Here we describe an approach to catalysis and the resulting development of an undirected, palladium-catalysed method for aromatic C-H fluorination using mild electrophilic fluorinating reagents. The reaction involves a mode of catalysis that is unusual in aromatic C-H functionalization because no organometallic intermediate is formed; instead, a reactive transition-metal-fluoride electrophile is generated catalytically for the fluorination of arenes that do not otherwise react with mild fluorinating reagents. The scope and functional-group tolerance of this reaction could provide access to functional fluorinated molecules in pharmaceutical and agrochemical development that would otherwise not be readily accessible.

DIRECT PALLADIUM-CATALYZED AROMATIC FLUORINATION

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Paragraph 00193, (2017/09/27)

Provided herein are palladium complexes comprising a ligand of Formula (Α') and a ligand of Formula (B), wherein R1-R18 are as defined herein. The palladium complexes are useful in methods of fluorinating aryl and heteroaryl substrates. Further provided are compositions and kits comprising the palladium complexes.

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