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

1438414-75-5

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1438414-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1438414-75-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,3,8,4,1 and 4 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1438414-75:
(9*1)+(8*4)+(7*3)+(6*8)+(5*4)+(4*1)+(3*4)+(2*7)+(1*5)=165
165 % 10 = 5
So 1438414-75-5 is a valid CAS Registry Number.

1438414-75-5Downstream Products

1438414-75-5Relevant 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 (2014/03/21)

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

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