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(4-fluoro-phenyl)-piperidin-1-yl-acetic acid ethyl ester is a complex organic compound with the molecular formula C16H22FNO2. It is a derivative of piperidine, an alkaloid found in many plants, and features a 4-fluoro-phenyl group attached to the piperidine ring. (4-fluoro-phenyl)-piperidin-1-yl-acetic acid ethyl ester is an ester, specifically an ethyl ester, which means it has an ethoxy group (-OCH2CH3) attached to the carboxylic acid group. It is a colorless liquid at room temperature and is soluble in organic solvents. This chemical has potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs, due to its unique structure and properties.

7550-18-7

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7550-18-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7550-18-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,5 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7550-18:
(6*7)+(5*5)+(4*5)+(3*0)+(2*1)+(1*8)=97
97 % 10 = 7
So 7550-18-7 is a valid CAS Registry Number.

7550-18-7Downstream Products

7550-18-7Relevant academic research and scientific papers

Copper activation of boronic acids: Factors affecting reactivity

Frauenlob, Robin,Garcia, Carlos,Butler, Susan,Bergin, Enda

, p. 432 - 435 (2014)

The generation of nucleophiles from the combination of aryl boronic acids and catalytic amounts of copper salt allows a reactivity distinct from other organometallic species, such as organolithiums or Grignard reagents. Here we examine how the electronic

A copper-catalyzed petasis reaction for the synthesis of tertiary amines and amino esters

Frauenlob, Robin,Garcia, Carlos,Bradshaw, Gary A.,Burke, Helen M.,Bergin, Enda

experimental part, p. 4445 - 4449 (2012/06/18)

We have developed a copper-catalyzed process for the coupling of aldehydes, amines, and boronic acids. This allows greater reactivity with simple aryl boronic acids and allows coupling reactions to proceed that previously failed. Initial mechanistic studi

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