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855654-26-1

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855654-26-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 855654-26-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,5,6,5 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 855654-26:
(8*8)+(7*5)+(6*5)+(5*6)+(4*5)+(3*4)+(2*2)+(1*6)=201
201 % 10 = 1
So 855654-26-1 is a valid CAS Registry Number.

855654-26-1Downstream Products

855654-26-1Relevant academic research and scientific papers

Palladium-Catalyzed, Ring-Forming Aromatic C-H Alkylations with Unactivated Alkyl Halides

Venning, Alexander R. O.,Bohan, Patrick T.,Alexanian, Erik J.

, p. 3731 - 3734 (2015)

A catalytic C-H alkylation using unactivated alkyl halides and a variety of arenes and heteroarenes is described. This ring-forming process is successful with a variety of unactivated primary and secondary alkyl halides, including those with β-hydrogens. In contrast to standard polar or radical cyclizations of aromatic systems, electronic activation of the substrate is not required. The mild, catalytic reaction conditions are highly functional group tolerant and facilitate access to a diverse range of synthetically and medicinally important carbocyclic and heterocyclic systems.

Radical Addition Enables 1,2-Aryl Migration from a Vinyl-Substituted All-Carbon Quaternary Center

Li, Zexian,Shi, Zhuangzhi,Wang, Minyan

supporting information, p. 186 - 190 (2020/11/02)

An efficient method for photocatalytic perfluoroalkylation of vinyl-substituted all-carbon quaternary centers involving 1,2-aryl migration has been developed. The rearrangement reactions use fac-Ir(ppy)3, visible light and commercially available fluoroalkyl halides and can generate valuable multisubstituted perfluoroalkylated compounds in a single step that would be challenging to prepare by other methods. Mechanistically, the photoinduced alkyl radical addition to an alkene leads to the migration of a vicinal aryl substituent from its adjacent all-carbon quaternary center with the concomitant generation of a C-radical bearing two electron-withdrawing groups that is further reduced by a hydrogen donor to complete the domino sequence.

Synthesis and pharmacological study of some new β-(dialkylaminomethyl)-γ-butyrolactones and their tetrahydrofuran analogues

Foscolos,Kolocouris,Fytas,Marakos,Pouli,Vamvakides

, p. 19 - 26 (2007/10/03)

This paper describes the synthesis of β-(dialkylaminomethyl)-γ-butyrolactones (6 and 15) and their tetrahydrofuran analogs 7 and 16. Their convulsant activity was studied on mice and could display an antiGABAergic component, but, unlike the α-(dialkylamin

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