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TCI

CAS 703-80-0

3-Acetylindole TCI A0849

3-Acetylindole TCI A0849

Chemical Identity

CAS No.
703-80-0
PubChem
CID 12802·SID 87562367
Formula
C10H9NO
Molecular weight
159.18 g/mol
Purity
>98.0%(N)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-(1H-indol-3-yl)ethanone
SMILES
CC(=O)C1=CNC2=CC=CC=C21
InChIKey
VUIMBZIZZFSQEE-UHFFFAOYSA-N
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3-Acetylindole is a chemical compound classified under the heterocyclic category, featuring an indole structure with an acetyl group at the 3-position. This compound plays a vital role in laboratory settings, particularly in the synthesis of complex molecules. It is widely used in organic and pharmaceutical research due to its ability to participate in various chemical reactions. Its structural versatility makes it a key building block for the development of compounds with specific biological activities.

The compound's high reactivity and complex molecular structure make it a preferred choice for chemists. It is capable of undergoing substitution and cyclization reactions, which are essential in the creation of new chemical entities. Its ability to react with different functional groups allows for the synthesis of a wide range of bioactive compounds. This reactivity, combined with its stability under controlled conditions, enhances its utility in both academic and industrial research.

In Indonesian laboratories, 3-Acetylindole is commonly used in chemical and pharmacological studies. It is frequently involved in experiments aimed at developing new compounds with pharmacological activities, such as antitumor agents. Its presence in research projects highlights its importance in advancing scientific knowledge and innovation in the field of chemistry.

  • Organic synthesis: 3-Acetylindole is widely used in organic synthesis due to its ability to participate in various reaction mechanisms, making it ideal for the development of complex molecular structures.
  • Pharmaceutical research: The compound is a valuable tool in pharmaceutical research for the synthesis of bioactive molecules with potential therapeutic applications.
  • Heterocyclic chemistry: Its indole core makes it a key component in the study of heterocyclic compounds, enabling the exploration of new chemical properties and reactivity patterns.
  • Drug discovery: 3-Acetylindole is often employed in drug discovery processes to create derivatives with enhanced biological activity and therapeutic potential.
  • Industrial chemical processes: It is used in industrial chemical processes as a building block for the production of specialty chemicals and intermediates.

Brand TCI
CAS number 703-80-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various pack sizes to meet different laboratory needs
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

3-Acetylindole should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care in a well-ventilated laboratory environment. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. It should be kept away from incompatible substances to avoid any potential chemical reactions. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.

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