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N-(2-iodophenyl)-N-(prop-2-yn-1-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119952-16-8

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119952-16-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119952-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,9,5 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119952-16:
(8*1)+(7*1)+(6*9)+(5*9)+(4*5)+(3*2)+(2*1)+(1*6)=148
148 % 10 = 8
So 119952-16-8 is a valid CAS Registry Number.

119952-16-8Relevant academic research and scientific papers

Asymmetric Domino Heck/Dearomatization Reaction of β-Naphthols to Construct Indole-Terpenoid Frameworks

Wang, Dong-Chao,Cheng, Peng-Peng,Yang, Ting-Ting,Wu, Pan-Pan,Qu, Gui-Rong,Guo, Hai-Ming

supporting information, p. 7865 - 7872 (2021/10/20)

A palladium-catalyzed enantioselective Heck cyclization/dearomatization cascade via capturing the cyclized Heck π-allylpalladium intermediate by β-naphthols is reported, which provides a new strategy for the construction of chiral indole-terpenoid framewo

Palladium-Catalyzed Domino Allenamide Carbopalladation/Direct C-H Allylation of Heteroarenes: Synthesis of Primprinine and Papaverine Analogues

Hédouin, Jonathan,Schneider, Cédric,Gillaizeau, Isabelle,Hoarau, Christophe

, p. 6027 - 6032 (2018/10/05)

Palladium-catalyzed intramolecular carbopalladation onto allenamides completed by direct C-H allylation of heterocycles is studied. The domino construction/heteroarylation of isoquinolone process is first achieved. A general three-step one-pot strategy, i

Chromium(II)-Mediated Nickel(II)-Catalysed Cyclisations of (Iodoaryl)-Substituted Alkynes and Alkynals

Hodgson, David M.,Wells, Christopher

, p. 1601 - 1604 (2007/10/02)

The Chromium(II)-mediated Nickel(II)-catalysed cyclisations of (iodoaryl)-substituted alkynes 1, 2 and 7 and (iodoaryl)-substituted alkynals 9 and 10 to give the products 5, 6, 8, 11 and 12 respectively is described.

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