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N-(3-fluorophenyl)methacrylamide is a synthetic chemical compound with the molecular formula C10H10FNO. It is a derivative of methacrylamide, featuring a 3-fluorophenyl group attached to the nitrogen atom. N-(3-fluorophenyl)methacrylamide is primarily used in the field of organic chemistry, particularly in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for a range of applications, including the development of new materials with specific properties. Due to its potential use in creating compounds with biological activity, it is also of interest in medicinal chemistry research.

1716-97-8

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1716-97-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1716-97-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,1 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1716-97:
(6*1)+(5*7)+(4*1)+(3*6)+(2*9)+(1*7)=88
88 % 10 = 8
So 1716-97-8 is a valid CAS Registry Number.

1716-97-8Relevant academic research and scientific papers

Copper-Catalyzed Radical N-Demethylation of Amides Using N-Fluorobenzenesulfonimide as an Oxidant

Yi, Xuewen,Yi, Xuewen,Lei, Siyu,Liu, Wangsheng,Che, Fengrui,Yu, Chunzheng,Liu, Xuesong,Wang, Zonghua,Zhou, Xin,Zhang, Yuexia

supporting information, p. 4583 - 4587 (2020/05/05)

An unprecedented N-demethylation of N-methyl amides has been developed by use of N-fluorobenzenesulfonimide as an oxidant with the aid of a copper catalyst. The conversion of amides to carbinolamines involves successive single-electron transfer, hydrogen-atom transfer, and hydrolysis, and is accompanied by formation of N-(phenylsulfonyl)benzenesulfonamide. Carbinolamines spontaneously decompose to N-demethylated amides and formaldehyde, because of their inherent instability.

Metal-free nitro-carbocyclization of activated alkenes: A direct approach to synthesize oxindoles by cascade C-N and C-C bond formation

Shen, Tao,Yuan, Yizhi,Jiao, Ning

supporting information, p. 554 - 556 (2014/01/06)

A novel and direct metal-free nitro-carbocyclization of activated alkenes leading to valuable nitro-containing oxindoles via cascade C-N and C-C bond formation has been developed. The mechanistic study indicates that the initial NO and NO2 radical addition and the following C-H functionalization processes are involved in this transformation. The Royal Society of Chemistry 2014.

Iron-catalyzed aerobic difunctionalization of alkenes: A highly efficient approach to construct oxindoles by C-S and C-C bond formation

Shen, Tao,Yuan, Yizhi,Song, Song,Jiao, Ning

supporting information, p. 4115 - 4118 (2014/04/03)

A novel iron-catalyzed efficient approach to construct sulfone-containing oxindoles, which play important roles in the structural library design and drug discovery, has been developed. The use of readily available benzenesulfinic acids, an inexpensive iron salt as the catalyst, and air as the oxidant makes this sulfur incorporation protocol very efficient and practical. This journal is the Partner Organisations 2014.

Ag-promoted azido-carbocyclization of activated alkenes via C - H bond cleavage

Yuan, Yizhi,Shen, Tao,Wang, Kui,Jiao, Ning

supporting information, p. 2932 - 2935 (2014/01/06)

A sliver of silver: An efficient silver-promoted azido-carbocyclization of activated alkenes via a radical pathway has been developed. Azido oxindoles, which hold great potential for subsequent transformation of the azido unit, are efficiently constructed by this protocol. Radical addition and C - H functionalization processes are involved in this transformation with the formation of C - N and C - C bonds. Silver is observed to promote the single-electron oxidation process. Copyright

Palladium-catalyzed oxidative arylalkylation of activated alkenes: Dual C-H bond cleavage of an arene and acetonitrile

Wu, Tao,Mu, Xin,Liu, Guosheng

supporting information; scheme or table, p. 12578 - 12581 (2012/02/04)

Not one but two: The title reaction proceeds through the dual C-H bond cleavage of both aniline and acetonitrile (see scheme). The reaction affords a variety of cyano-bearing indolinones in excellent yield. Mechanistic studies demonstrate that this reaction involves a fast arylation of the olefin and a rate-determining C-H activation of the acetonitrile. Copyright

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