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1322084-98-9

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1322084-98-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1322084-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,2,0,8 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1322084-98:
(9*1)+(8*3)+(7*2)+(6*2)+(5*0)+(4*8)+(3*4)+(2*9)+(1*8)=129
129 % 10 = 9
So 1322084-98-9 is a valid CAS Registry Number.

1322084-98-9Relevant academic research and scientific papers

Enantioconvergent Amination of Racemic Tertiary C-H Bonds

Lang, Kai,Li, Chaoqun,Kim, Isaac,Zhang, X. Peter

supporting information, p. 20902 - 20911 (2020/12/22)

Racemization is considered to be an intrinsic stereochemical feature of free radical chemistry as can be seen in traditional radical halogenation reactions of optically active tertiary C-H bonds. If the facile process of radical racemization could be effe

Isomerization of olefins triggered by rhodium-catalyzed C-H bond activation: Control of endocyclic β-hydrogen elimination

Yip, Stephanie Y. Y.,A?ssa, Christophe

supporting information, p. 6870 - 6873 (2015/06/02)

Five-membered metallacycles are typically reluctant to undergo endocyclic β-hydrogen elimination. The rhodium-catalyzed isomerization of 4-pentenals into 3-pentenals occurs through this elementary step and cleavage of two C-H bonds, as supported by deuterium-labeling studies. The reaction proceeds without decarbonylation, leads to trans olefins exclusively, and tolerates other olefins normally prone to isomerization. Endocyclic β-hydrogen elimination can also be controlled in an enantiodivergent reaction on a racemic mixture.

Palladium-catalyzed haloallylation of aromatic ynol ethers with allyl chlorides: A highly regio- and stereoselective approach to (1E)-α- chloroenol ethers

Cai, Haiting,Yuan, Zheliang,Zhu, Weidong,Zhu, Gangguo

scheme or table, p. 8682 - 8684 (2011/09/15)

Described herein is a Pd-catalyzed haloallylation of aromatic ynol ethers and allyl chlorides, allowing facile access to (1E)-α-chloroenol ethers in a highly regio- and stereoselective manner. The synthetic utility of this method is demonstrated well by t

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