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TCI

CAS 771-51-7

3-Indoleacetonitrile TCI I0024

3-Indoleacetonitrile TCI I0024

Chemical Identity

Other names
IAN
CAS No.
771-51-7
PubChem
CID 351795·SID 87571433
Formula
C10H8N2
Molecular weight
156.18 g/mol
Purity
>98.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(1H-indol-3-yl)acetonitrile
SMILES
C1=CC=C2C(=C1)C(=CN2)CC#N
InChIKey
DMCPFOBLJMLSNX-UHFFFAOYSA-N
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3-Indoleacetonitrile is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds. It serves as a fundamental building block in organic chemistry, playing a crucial role in the development of complex molecular structures. This compound is particularly valuable in research focused on creating bioactive molecules, such as alkaloids and aromatic compounds, due to its unique molecular framework. Its versatility makes it an essential reagent for chemists working on drug discovery and synthetic chemistry projects.

The chemical properties of 3-Indoleacetonitrile make it a preferred choice for various synthetic reactions. It exhibits stability under specific conditions and can react with a range of reagents, including alkali metals and nitrogen-containing compounds. Its ability to participate in substitution and cyclization reactions enhances its utility in organic synthesis. The compound’s complex molecular structure allows it to be a key player in the formation of heterocyclic systems, which are common in pharmaceutical and medicinal chemistry.

In Indonesian laboratories, 3-Indoleacetonitrile is commonly used in organic chemistry research, especially in pharmacology and biomedical compound synthesis. It is a critical component in studies aimed at developing new drugs and bioactive materials. Its relevance extends to research requiring complex heterocyclic structures, making it a valuable resource for scientists working in academic and industrial settings.

  • Organic synthesis of heterocyclic compounds due to its structural complexity and reactivity.
  • Pharmaceutical research for the development of bioactive molecules and alkaloid derivatives.
  • Medicinal chemistry applications in the synthesis of aromatic and nitrogen-containing compounds.
  • Drug discovery projects requiring stable and reactive building blocks for molecular design.
  • Biomedical compound synthesis where heterocyclic structures are essential for biological activity.

Brand TCI
CAS number 771-51-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid or liquid depending on formulation
Storage Store in a cool, dry place away from light and moisture

3-Indoleacetonitrile should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with strong acids or bases, as these can cause unwanted chemical reactions. The compound should be stored away from incompatible substances to ensure safety in the laboratory. Proper labeling and storage conditions are essential to maintain its integrity and ensure safe handling.

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