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TCI

CAS 392-13-2

5-Fluoro-3-methylindole TCI F1053

5-Fluoro-3-methylindole TCI F1053

Chemical Identity

CAS No.
392-13-2
PubChem
CID 22351503·SID 354333715
Formula
C9H8FN
Molecular weight
149.17 g/mol
Purity
>98.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
5-fluoro-3-methyl-1H-indole
SMILES
CC1=CNC2=C1C=C(C=C2)F
InChIKey
CSDHAGJNOQIBHZ-UHFFFAOYSA-N
MDL
MDL03095377
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5-Fluoro-3-methylindole is a chemical compound widely used in organic reactions for the synthesis of complex molecules. As a fluorinated building block, it serves as a fundamental component in the development of more intricate chemical structures. This compound is particularly valuable in research settings where the creation of new substances with specific functional properties is required. Its versatility makes it a key player in the field of synthetic chemistry, enabling researchers to explore a wide range of chemical transformations.

The compound’s stable molecular structure and controlled reactivity make it a preferred choice for laboratory use. The presence of both fluorine and methyl groups allows for tailored chemical modifications, enhancing its applicability in various synthetic pathways. Its ability to participate in substitution, addition, and cyclization reactions further expands its utility. These characteristics render it highly sought after by chemists aiming to design new compounds with pharmaceutical, industrial, or analytical applications.

In Indonesian laboratories, 5-Fluoro-3-methylindole is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and indole derivatives. Its relevance spans across pharmaceutical, material science, and analytical chemistry fields. Due to its unique properties, it is a favored material for researchers working on the development of novel substances with potential applications in multiple industries.

  • Organic synthesis of heterocyclic compounds due to its structural versatility and reactivity.
  • Development of pharmaceutical compounds through targeted chemical modifications and functional group manipulations.
  • Research in material science for the creation of novel polymers and functional materials.
  • Analytical chemistry applications where precise molecular structures are required for compound identification.
  • Indole derivative synthesis, leveraging its stable molecular framework for complex chemical transformations.

Brand TCI
CAS number 392-13-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes 50g, 250g, 1kg
Physical form Crystalline solid
Storage Store in a cool, dry place away from light and moisture

5-Fluoro-3-methylindole should be stored in a cool, dry place, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. The compound is generally stable under normal laboratory conditions but should be handled with care to avoid contamination. Proper ventilation is advised during handling to ensure a safe working environment. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, to minimize potential exposure. Regular monitoring of storage conditions is essential to maintain the compound’s integrity and ensure its effectiveness in research applications.

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