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methyl (E)-3-(2-acetamido-5-fluorophenyl)acrylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1259100-53-2

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1259100-53-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1259100-53-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,9,1,0 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1259100-53:
(9*1)+(8*2)+(7*5)+(6*9)+(5*1)+(4*0)+(3*0)+(2*5)+(1*3)=132
132 % 10 = 2
So 1259100-53-2 is a valid CAS Registry Number.

1259100-53-2Downstream Products

1259100-53-2Relevant articles and documents

Pd(TFA)2-catalyzed oxidative coupling of anilides with olefins through C[sbnd]H bond activation under non-acidic conditions

Yu, Xiaoli,Yao, Wei,Wan, Huida,Xu, Zhaojun,Wang, Dawei

, p. 100 - 103 (2016)

C[sbnd]H bond activation is an important issue. The Pd-catalyzed and non-coordinating anion improved C[sbnd]H bond activation was realized through the oxidative coupling reaction of anilides with olefins under non-acidic conditions. Additionally, the cata

Non-coordinating-Anion-Directed Reversal of Activation Site: Selective C?H Bond Activation of N-Aryl Rings

Wang, Dawei,Yu, Xiaoli,Xu, Xiang,Ge, Bingyang,Wang, Xiaoli,Zhang, Yaxuan

, p. 8663 - 8668 (2016/07/07)

An Rh-catalyzed selective C?H bond activation of diaryl-substituted anilides is described. In an attempt to achieve C?H activation of C-aryl rings, we unexpectedly obtained an N-aryl ring product under non-coordinating anion conditions, whereas the C-aryl

Rhodium(III)-catalyzed internal oxidative coupling of N-hydroxyanilides with alkenes via C-H activation

Wen, Jing,Wu, An,Chen, Pei,Zhu, Jin

, p. 5282 - 5286 (2015/08/26)

Abstract Described herein is an efficient new method for ortho-olefination of anilides in the presence of AgSbF6 and NaOAc via rhodium(III)-catalyzed internal oxidative C-H bond activation based on hydroxyl as directing and oxidative group. A range of alkenes and functional groups on acetanilides is supported and a possible mechanism is proposed according to the experimental results.

Highly effective Pd-catalyzed ortho olefination of acetanilides: Broad substrate scope and high tolerability

Kim, Byung Seok,Jang, Chungsik,Lee, Dong Jin,Youn, So Won

, p. 2336 - 2340 (2011/06/25)

Bring it on! An effective Pd-catalyzed ortho olefination of various acetanilides has been developed. This transformation has a broad substrate scope and wide functional-group tolerability, regardless of the electronic and steric properties of acetanilide substrates, providing a straightforward access to highly functionalized arenes.

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