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4-methoxy-3-[(4-methylphenyl)thio]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1622221-66-2

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1622221-66-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1622221-66-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,2,2,2 and 1 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1622221-66:
(9*1)+(8*6)+(7*2)+(6*2)+(5*2)+(4*2)+(3*1)+(2*6)+(1*6)=122
122 % 10 = 2
So 1622221-66-2 is a valid CAS Registry Number.

1622221-66-2Downstream Products

1622221-66-2Relevant academic research and scientific papers

Preparation method of indole sulfide compound

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Paragraph 0074-0078, (2019/05/08)

The invention discloses a preparation method of an indole sulfide compound. The preparation method is conducted according to the following steps that a catalyst, an indole reactant, hydrazine hydrate,substituted phenyl sulfonyl chloride and a solvent are

Copper-catalyzed aerobic oxidative N-S bond functionalization for C-S bond formation: Regio- and stereoselective synthesis of sulfones and thioethers

Li, Xianwei,Xu, Yanli,Wu, Wanqing,Jiang, Chang,Qi, Chaorong,Jiang, Huanfeng

supporting information, p. 7911 - 7915 (2014/07/07)

A regio- and stereoselective synthesis of sulfones and thioethers by means of CuI-catalyzed aerobic oxidative N-S bond cleavage of sulfonyl hydrazides, followed by cross-coupling reactions with alkenes and aromatic compounds to form the C-sp-2-S bond, is described herein. N2 and H2O are the byproducts of this transformation, thus offering an environmentally benign process with a wide range of potential applications in organic synthesis and medicinal chemistry. First cleave, then cross-couple: A direct Cu-catalyzed aerobic oxidative C-sp-2-H functionalization and C-S bond coupling reaction has been developed (see scheme). By slight modification of the additive, sulfonyl hydrazides could serve as sulfonation, sulfenation, or arylation reagents to undergo cross-coupling reactions with alkenes and (hetero)aromatic cycles, affording sulfones, thioethers, and biaryl compounds with high regio- and stereoselectivities (see scheme).

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