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3,3-difluoro-2-(4-methoxyphenyl)-3H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1402604-36-7

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1402604-36-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1402604-36-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,6,0 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1402604-36:
(9*1)+(8*4)+(7*0)+(6*2)+(5*6)+(4*0)+(3*4)+(2*3)+(1*6)=107
107 % 10 = 7
So 1402604-36-7 is a valid CAS Registry Number.

1402604-36-7Downstream Products

1402604-36-7Relevant academic research and scientific papers

Aminofluorination of 2-alkynylanilines: A Au-catalyzed entry to fluorinated indoles

Arcadi, Antonio,Pietropaolo, Emanuela,Alvino, Antonello,Michelet, Veronique

, p. 449 - 458 (2014)

The scope and limitations of gold-catalyzed tandem cycloisomerization/ fluorination reactions of unprotected 2-alkynylanilines to have access to 3,3-difluoro-2-aryl-3H-indoles and 3-fluoro-2-arylindoles are described. An unprecedented aminoauration/oxidation/ fluorination cascade reaction of 2-alkynylanilines bearing a linear alkyl group on the terminal triple bond is reported.

Silver-catalyzed one-pot cyclization/fluorination of 2-alkynylanilines: Highly efficient synthesis of structurally diverse fluorinated indole derivatives

Yang, Lei,Ma, Yuanhong,Song, Feijie,You, Jingsong

supporting information, p. 3024 - 3026 (2014/03/21)

Highly efficient approaches to obtain structurally diverse fluorinated indole derivatives have been realized through the Ag-catalyzed one-pot cyclization/fluorination of 2-alkynylanilines in the presence of NFSI or Selectfluor. The Royal Society of Chemistry.

One-pot gold-catalyzed aminofluorination of unprotected 2-alkynylanilines

Arcadi, Antonio,Pietropaolo, Emanuela,Alvino, Antonello,Michelet, Véronique

supporting information, p. 2766 - 2769 (2013/07/19)

A tandem gold(I)-catalyzed aminocylization/fluorination and a two-step, one-pot gold(III)-catalyzed cyclization/electrophilic fluorination provide a convenient and general method for the synthesis of 3,3-difluoro-2-substituted- 3H-indoles in good yield un

Exploration of forbidden povarov processes as a source of unexpected reactivity: A multicomponent Mannich-Ritter transformation

Preciado, Sara,Vicente-García, Esther,Llabrés, Salomé,Luque, F. Javier,Lavilla, Rodolfo

supporting information; experimental part, p. 6874 - 6877 (2012/10/08)

When a door closes, a window opens! The use of geometrically or electronically restricted imines for Povarov-type processes does not afford the anti-Bredt tetrahydroquinolines, but leads instead to highly functionalized structures through novel reaction pathways (see picture; LA=Lewis acid). The exploration of forbidden routes constitutes a valuable approach in the search for new multicomponent reactions. Copyright

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