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CAS 773-91-1

5-Fluoro-1-methylindoline-2,3-dione TCI F1390

5-Fluoro-1-methylindoline-2,3-dione TCI F1390

Chemical Identity

Other names
5-Fluoro-1-methyl-1H-indole-2,3-dione · 5-Fluoro-1-methylisatin · 5-Fluoro-N-methylisatin
CAS No.
773-91-1
PubChem
CID 1818553
Formula
C9H6FNO2
Molecular weight
179.15 g/mol
Purity
>98.0%(GC)(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
5-fluoro-1-methylindole-2,3-dione
SMILES
CN1C2=C(C=C(C=C2)F)C(=O)C1=O
InChIKey
VHJRLOILUKMNEY-UHFFFAOYSA-N
MDL
MDL02956480
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5-Fluoro-1-methylindoline-2,3-dione is a fluorinated building block widely used in organic chemistry for the synthesis of complex molecules. This compound plays a crucial role in laboratory settings where researchers aim to create heterocyclic structures and indole derivatives. As a key component in the field of fluorinated compounds, it is valued for its ability to participate in various chemical reactions, particularly those involving substitution and structural modification. Its unique chemical structure, featuring both fluorine and methyl groups, contributes to its reactivity and versatility in synthetic pathways.

The compound’s fluorine atoms significantly influence its polarity and reactivity, making it a preferred choice for chemists working on drug development and organic synthesis. The presence of fluorine enhances the compound’s stability and functional group compatibility, allowing for greater control over reaction outcomes. Its molecular framework also supports the design of bioactive molecules, which are essential in pharmaceutical research. These properties make it a reliable and effective reagent for advanced chemical applications.

In Indonesian laboratories, 5-Fluoro-1-methylindoline-2,3-dione is commonly used by chemists and pharmacologists to develop new compounds with specific biological activities. Its role in the synthesis of therapeutic agents and other complex molecules makes it a valuable resource in both academic and industrial research environments. Researchers rely on its predictable behavior and chemical versatility to achieve precise results in their experiments.

  • Organic synthesis of heterocyclic compounds due to its fluorinated structure and reactivity.
  • Development of pharmaceutical compounds as a building block for bioactive molecule design.
  • Structural modification of indole derivatives in medicinal chemistry research applications.
  • Synthesis of complex molecules requiring fluorine substitution in organic reaction pathways.
  • Use in academic and industrial research for creating novel chemical entities with therapeutic potential.

Brand TCI
CAS number 773-91-1
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid (may vary depending on supplier)
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Proper ventilation should be maintained in the laboratory when handling the material to minimize inhalation risks. As a fluorinated compound, it is important to follow standard chemical safety protocols, including the use of personal protective equipment such as gloves and safety goggles. The compound is generally stable under normal laboratory conditions but should be handled with care to avoid contamination or unintended chemical interactions.

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