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3-Fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile
[CAS# 1672665-55-2]

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Identification
ClassificationOrganic raw materials >> Organic fluorine compound >> Fluorobenzonitrile series
Name3-Fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile
Molecular StructureCAS # 1672665-55-2, 3-Fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile
Molecular FormulaC17H12FNO4S
Molecular Weight345.34
CAS Registry Number1672665-55-2
EC Number875-702-0
SMILESCS(=O)(=O)C1=C2C(=C(C=C1)OC3=CC(=CC(=C3)C#N)F)CCC2=O
Properties
Density1.5±0.1 g/cm3, Calc.*
Index of Refraction1.636, Calc.*
Boiling Point550.0±50.0 °C (760 mmHg), Calc.*
Flash Point286.4±30.1 °C, Calc.*
*Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbolssymbol   GHS07 Warning  Details
Risk StatementsH302-H315-H319  Details
Safety StatementsP501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330  Details
SDSAvailable
up Discovery and Applications
3-Fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile is an important synthetic compound with significant applications in medicinal chemistry. The discovery of this molecule stemmed from efforts to develop selective inhibitors for various kinases involved in cancer and inflammatory diseases. Its structure, featuring a fluoro-benzonitrile moiety linked to a methylsulfonyl indanone, enhances binding specificity and metabolic stability.

The synthesis of 3-fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile involves multi-step procedures, including nucleophilic aromatic substitution and sulfonylation reactions. The strategic introduction of the fluoro and benzonitrile groups provides the molecule with high electrophilicity, improving its interaction with target proteins. These synthetic steps ensure the production of high-purity compounds necessary for pharmaceutical applications.

This compound is widely studied as a lead candidate in the design of kinase inhibitors for the treatment of cancers and autoimmune conditions. Its role in modulating cellular signaling pathways has shown potential for reducing tumor growth and inflammatory responses. The chemical stability and bioavailability of 3-fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile make it an attractive candidate for further drug development.

Ongoing research focuses on optimizing the pharmacokinetic properties of this molecule to enhance its therapeutic efficacy. The exploration of derivatives and analogs continues to expand the potential applications of this compound in various areas of medical research.

References

2022. Synthesis of Belzutifan. Synfacts.
DOI: 10.1055/s-0041-1738315
Market Analysis Reports
List of Reports Available for 3-Fluoro-5-((7-(methylsulfonyl)-1-oxo-2,3-dihydro-1H-inden-4-yl)oxy)benzonitrile
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