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Home  > 1-(Phenylsulphonyl)-2-chloro-7-azaindole

AA24562

1227268-62-3 | 1-(Phenylsulphonyl)-2-chloro-7-azaindole

Packsize Purity Availability Price Discounted Price    Quantity
100mg 97% 2 weeks $50.00 $35.00 -   +
250mg 97% 2 weeks $67.00 $47.00 -   +
1g 97% 2 weeks $163.00 $114.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA24562
Chemical Name: 1-(Phenylsulphonyl)-2-chloro-7-azaindole
CAS Number: 1227268-62-3
Molecular Formula: C13H9ClN2O2S
Molecular Weight: 292.7408
MDL Number: MFCD16875829
SMILES: Clc1cc2c(n1S(=O)(=O)c1ccccc1)nccc2

 

Upstream Synthesis Route
  • 2-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine, also known as $name$, is a versatile chemical compound that finds wide applications in chemical synthesis. This compound serves as an important building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable reagent in organic synthesis processes.The 2-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine is commonly used as a key intermediate in the construction of complex heterocyclic compounds due to its ability to undergo various functional group transformations. Its substitution pattern allows for selective modifications, making it a valuable tool in designing and synthesizing new molecules with desired properties.In chemical synthesis, this compound acts as a versatile nucleophilic and electrophilic reactant, participating in diverse reactions such as Suzuki coupling, Sonogashira coupling, and Buchwald-Hartwig amination. These reactions enable the incorporation of the 2-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine moiety into more intricate structures, enhancing the overall molecular complexity and diversity of the final products.Moreover, the presence of a chloro group in this compound provides opportunities for further derivatization and functionalization, allowing for the introduction of additional substituents or structural motifs. This flexibility in chemical modification makes 2-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine a valuable component in the synthesis of diverse organic compounds with tailored properties and functionalities.
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