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N-phenyl-N-(propa-1,2-dien-1-yl)methanesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1369999-89-2

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1369999-89-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1369999-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,9,9 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1369999-89:
(9*1)+(8*3)+(7*6)+(6*9)+(5*9)+(4*9)+(3*9)+(2*8)+(1*9)=262
262 % 10 = 2
So 1369999-89-2 is a valid CAS Registry Number.

1369999-89-2Relevant academic research and scientific papers

Ligand-Controlled Regiodivergence for Catalytic Stereoselective Semireduction of Allenamides

Hajiloo Shayegan, Mojtaba,Li, Zhong-Yuan,Cui, Xin

, (2021/12/02)

Ligand-controlled regiodivergence has been developed for catalytic semireduction of allenamides with excellent chemo- and stereocontrol. This system also provides an example of catalytic regiodivergent semireduction of allenes for the first time. The divergence of the semireduction is enabled by ligand switch with the same palladium pre-catalyst under operationally simple and mild conditions. Monodentate ligand XPhos exclusively promotes selective 1,2-semireduction to afford allylic amides, while bidentate ligand BINAP completely switched the regioselectivity to 2,3-semireduction, producing (E)-enamide derivatives.

Dynamic Kinetic Resolution in Gold-Catalyzed (4 + 2)-Annulations between Alkynyl Benzaldehydes and Allenamides to Yield Enantioenriched All-Carbon Diarylalkylmethane Derivatives

Pandit, Yashwant Bhaskar,Liu, Rai-Shung

supporting information, p. 548 - 553 (2022/01/20)

This work reports the synthesis of diarylmethane derivatives via gold-catalyzed (4 + 2)-annulations between alkynyl benzaldehydes and allenamides, followed by an aza-Claisen rearrangement. Deuterium labeling and crossover experiments have been performed to confirm this proposed mechanism. With racemic 3-substituted allenamides in a substrate ratio (1:1), we employ chiral gold catalysts to achieve a dynamic kinetic resolution to obtain enantioenriched diarylalkylmethane derivatives with high e.r. levels (up to 93:7).

Gold-Catalyzed Intermolecular Formal [4 + 2 + 2]-Cycloaddition of Anthranils with Allenamides

Wang, Cheng,Xu, Guangyang,Shao, Ying,Tang, Shengbiao,Sun, Jiangtao

supporting information, p. 5990 - 5994 (2020/08/12)

The construction of eight-membered rings is a challenging issue due to unfavorable transannular strain and entropic barriers. We report herein a gold-catalyzed formal [4 + 2 + 2] cycloaddition reaction of anthranils with allenamides to deliver oxa-bridged eight-membered heterocycles in accepted yields with unique E/Z configuration. Moreover, the asymmetric [4 + 2 + 2] cycloaddition by using chiral phosphoramidite gold catalyst has also been conducted.

A palladium-catalyzed regiocontrollable hydroarylation reaction of allenamides with B2pin2/H2O

Cui, Jie,Meng, Long,Chi, Xiaochen,Liu, Qing,Zhao, Pingping,Zhang, Dao-Peng,Chen, Lei,Li, Xinjin,Dong, Yunhui,Liu, Hui

, p. 4355 - 4358 (2019/04/26)

A novel palladium-catalyzed regiocontrollable hydroarylation reaction of allenamides with B2pin2/H2O has been disclosed. H2O as an ideal hydrogen source was activated by B2pin2 to furnish allylamines or enamines with a broad functional group tolerance. The regioselectivity for both of the two products was up to 99:1 for most of the examples, which was achieved by adjusting the addition order of the catalyst and iodobenzene derivatives. The tentative investigation of the mechanism proved the reaction to be a non-radical process and the deuterium-labeled experiments indicated that the hydrogen was from H2O.

Synthesis of allyl acetates via palladium-catalysed functionalisation of allenes and 1,3-dienes

Husinec, Suren,Petkovic, Milos,Savic, Vladimir,Simic, Milena

experimental part, p. 399 - 408 (2012/03/11)

-Allylpalladium intermediates are known to participate efficiently in transformations involving nucleophilic species. Exploring these processes, we have developed a method for the preparation of allyl acetates via palladium-catalysed functionalisation of

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