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AB45421

324-03-8 | 6-Fluoroisatin

Packsize Purity Availability Price Discounted Price    Quantity
5g 98% in stock $11.00 $8.00 -   +
10g 98% in stock $20.00 $14.00 -   +
25g 98% in stock $49.00 $35.00 -   +
100g 98% in stock $195.00 $137.00 -   +

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

*All prices are in USD.

Description
Catalog Number: AB45421
Chemical Name: 6-Fluoroisatin
CAS Number: 324-03-8
Molecular Formula: C8H4FNO2
Molecular Weight: 165.1213
MDL Number: MFCD03618556
SMILES: Fc1ccc2c(c1)NC(=O)C2=O
NSC Number: 650911

 

Computed Properties
Complexity: 241  
Covalently-Bonded Unit Count: 1  
Heavy Atom Count: 12  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
XLogP3: 0.7  

 

 

Upstream Synthesis Route
  • 6-Fluoroindoline-2,3-dione is a highly versatile compound that finds significant utility in organic synthesis processes. This compound serves as a valuable building block in the creation of diverse chemical structures and functionalities due to its unique reactivity and molecular properties.One of the primary applications of 6-Fluoroindoline-2,3-dione in chemical synthesis is its role as a key intermediate in the preparation of various heterocyclic compounds. By undergoing different reactions and transformations, this compound can be utilized to introduce fluorine atoms into organic molecules, which is essential for enhancing their biological activity or altering their physical properties.Furthermore, 6-Fluoroindoline-2,3-dione serves as a precursor in the synthesis of novel pharmaceuticals, agrochemicals, and materials. Its ability to participate in diverse chemical reactions, such as substitution, addition, and cyclization reactions, makes it a valuable tool for designing and developing new compounds with desired properties and functions.Overall, the strategic incorporation of 6-Fluoroindoline-2,3-dione in chemical synthesis processes enables researchers and synthetic chemists to access a wide range of molecular scaffolds and functional groups, thereby facilitating the discovery of new compounds with potential applications in various fields of chemistry and beyond.
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