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N-(1,3-dihydro-2-benzofuran-1-yl)-4-toluenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1423124-47-3

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1423124-47-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1423124-47-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,3,1,2 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1423124-47:
(9*1)+(8*4)+(7*2)+(6*3)+(5*1)+(4*2)+(3*4)+(2*4)+(1*7)=113
113 % 10 = 3
So 1423124-47-3 is a valid CAS Registry Number.

1423124-47-3Downstream Products

1423124-47-3Relevant academic research and scientific papers

A Metal–Organic Framework with Exceptional Activity for C?H Bond Amination

Wang, Le,Agnew, Douglas W.,Yu, Xiao,Figueroa, Joshua S.,Cohen, Seth M.

, p. 511 - 515 (2018/02/21)

The development of catalysts capable of fast, robust C?H bond amination under mild conditions is an unrealized goal despite substantial progress in the field of C?H activation in recent years. A Mn-based metal–organic framework (CPF-5) is described that promotes the direct amination of C?H bonds with exceptional activity. CPF-5 is capable of functionalizing C?H bonds in an intermolecular fashion with unrivaled catalytic stability producing >105 turnovers.

Enantioselective, intermolecular benzylic C-H amination catalysed by an engineered iron-haem enzyme

Prier, Christopher K.,Zhang, Ruijie K.,Buller, Andrew R.,Brinkmann-Chen, Sabine,Arnold, Frances H.

, p. 629 - 634 (2017/06/30)

C-H bonds are ubiquitous structural units of organic molecules. Although these bonds are generally considered to be chemically inert, the recent emergence of methods for C-H functionalization promises to transform the way synthetic chemistry is performed. The intermolecular amination of C-H bonds represents a particularly desirable and challenging transformation for which no efficient, highly selective, and renewable catalysts exist. Here we report the directed evolution of an iron-containing enzymatic catalyst - based on a cytochrome P450 monooxygenase - for the highly enantioselective intermolecular amination of benzylic C-H bonds. The biocatalyst is capable of up to 1,300 turnovers, exhibits excellent enantioselectivities, and provides access to valuable benzylic amines. Iron complexes are generally poor catalysts for C-H amination: in this catalyst, the enzyme's protein framework confers activity on an otherwise unreactive iron-haem cofactor.

Syntheses of a novel fluorinated trisphosphinoborate ligand and its copper and silver complexes. Catalytic activity toward nitrene transfer reactions

Arenas, Ismael,Fuentes, M. Angeles,Alvarez, Eleuterio,Diaz, Yolanda,Caballero, Ana,Castillon, Sergio,Perez, Pedro J.

, p. 3991 - 3999 (2014/05/06)

A novel fluorinated ligand, the anionic PhB(CH2P(p-CF 3C6H4)2)3 (PhBP 3 p-CF3Ph), has been synthesized and characterized, as well as its corresponding thallium, copper

Transition-metal-free benzylic C-H bond intermolecular amination utilizing chloramine-T and I2

Takeda, Youhei,Hayakawa, Junpei,Yano, Kazuki,Minakata, Satoshi

supporting information, p. 1672 - 1674 (2013/02/23)

An intermolecular benzylic C-H bond amination utilizing the combination of chloramine-T and I2 without the aid of transition-metal catalysts has been developed. The reaction was found applicable to a variety of benzene-substituted alkanes, as w

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