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1093759-51-3

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1093759-51-3 Usage

Purity

97%

Structural Features

Contains a benzyl group
Contains an iodine atom

Classification

Derivative of azaindole

Applications

Building blocks for the synthesis of biologically active compounds
Used in the field of drug discovery
Potential applications in medicinal chemistry and pharmaceutical research

Utilization

Key intermediate in the synthesis of new drug candidates
Reference standard for analytical purposes
These properties and specific content are based on the information provided, which highlights the compound's purity, structural features, and potential applications in the field of drug discovery and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1093759-51-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,3,7,5 and 9 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1093759-51:
(9*1)+(8*0)+(7*9)+(6*3)+(5*7)+(4*5)+(3*9)+(2*5)+(1*1)=183
183 % 10 = 3
So 1093759-51-3 is a valid CAS Registry Number.

1093759-51-3 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
  • Packaging
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  • Alfa Aesar

  • (H51675)  1-Benzyl-3-iodo-7-azaindole, 97%   

  • 1093759-51-3

  • 5g

  • 1764.0CNY

  • Detail

1093759-51-3Downstream Products

1093759-51-3Relevant articles and documents

Halogen Bond-Assisted Electron-Catalyzed Atom Economic Iodination of Heteroarenes at Room Temperature

Kazi, Imran,Guha, Somraj,Sekar, Govindasamy

, p. 6642 - 6654 (2019)

A halogen bond-assisted electron-catalyzed iodination of heteroarenes has been developed for the first time under atom economic condition at room temperature. The iodination is successful with just 0.55 equiv of iodine and 0.50 equiv of peroxide. The kinetic study indicates that the reaction is elusive in the absence of a halogen bond between the substrate and iodine. The formation of a halogen bond, its importance in lowering the activation barrier for this reaction, the presence of radical intermediates in a reaction mixture, and the regioselectivity of the reaction have been demonstrated with several control experiments, spectroscopic analysis, and quantum chemical calculations. Allowing the formation of the halogen bond may offer a new strategy to generate the reactive radical intermediates and to enable the otherwise elusive electron-catalyzed reactions under mild reaction conditions.

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