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Home  > Chemistry  > Heterocyclic Building Blocks  > Indolines  > 6-Fluorooxindole

AI52652

56341-39-0 | 6-Fluorooxindole

Packsize Purity Availability Price Discounted Price    Quantity
250mg 97% in stock $14.00 $10.00 -   +
1g 97% in stock $20.00 $14.00 -   +
5g 97% in stock $22.00 $16.00 -   +
10g 97% in stock $43.00 $31.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AI52652
Chemical Name: 6-Fluorooxindole
CAS Number: 56341-39-0
Molecular Formula: C8H6FNO
Molecular Weight: 151.1377
MDL Number: MFCD00047212
SMILES: O=C1Cc2c(N1)cc(cc2)F

 

Computed Properties
Complexity: 183  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 11  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 1  
XLogP3: 1.3  

 

 

Upstream Synthesis Route
  • 6-Fluoroindolin-2-one is a versatile organic compound that finds wide applications in chemical synthesis, particularly in the field of medicinal and pharmaceutical chemistry. This compound serves as a key building block in the synthesis of various biologically active molecules and pharmaceuticals due to its unique structure and reactivity.One of the main applications of 6-Fluoroindolin-2-one is as a synthon for the construction of heterocyclic compounds. Its fluorinated moiety imparts specific properties to the resulting molecules, making them potential candidates for drug development. By utilizing 6-Fluoroindolin-2-one as a starting material, chemists can access a diverse range of complex structures through various synthetic strategies such as cyclization reactions, functional group manipulations, and cross-coupling reactions.Moreover, the presence of the indolin-2-one scaffold in 6-Fluoroindolin-2-one offers a platform for further derivatization, allowing for the introduction of different functional groups or modifications to tailor the physicochemical and biological properties of the final compounds. This flexibility in structural modification makes 6-Fluoroindolin-2-one a valuable tool in the design and synthesis of novel drug candidates with enhanced pharmacological profiles.Overall, the application of 6-Fluoroindolin-2-one in chemical synthesis opens up possibilities for the creation of diverse molecular structures with potential applications in drug discovery, agrochemicals, and materials science. Its role as a key intermediate highlights its importance in the development of new bioactive compounds and underscores its significance in modern organic synthesis methodologies.
Literature
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