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TCI

CAS 942-24-5

Methyl Indole-3-carboxylate TCI I0491

Methyl Indole-3-carboxylate TCI I0491

Chemical Identity

CAS No.
942-24-5
PubChem
CID 589098·SID 87571840
Formula
C10H9NO2
Molecular weight
175.18 g/mol
Purity
>98.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 1H-indole-3-carboxylate
SMILES
COC(=O)C1=CNC2=CC=CC=C21
InChIKey
QXAUTQFAWKKNLM-UHFFFAOYSA-N
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Methyl Indole-3-carboxylate is a chemical compound widely used in organic reactions for the synthesis of heterocyclic compounds. It serves as a key building block in the creation of indole-based structures, which are fundamental in both pharmaceutical and material sciences. This compound is commonly found in chemical laboratories as a raw material for the development of complex molecules with diverse applications. Its role as a precursor allows it to participate in various reactions, making it indispensable in synthetic chemistry workflows.

The stability of its chemical structure and its good reactivity make Methyl Indole-3-carboxylate a preferred choice for laboratory use. It can readily react with a variety of reagents, enabling the formation of a wide range of functional groups. This versatility allows chemists to tailor the final product according to specific research needs. Additionally, its ability to form bonds with different functional groups enhances its utility in creating structurally diverse compounds, which is crucial for drug development and material innovation.

In Indonesian laboratories, Methyl Indole-3-carboxylate is frequently used in organic chemistry research, particularly in the development of new compounds with potential medical or industrial applications. Its availability ensures that researchers can meet the demands of experiments requiring high-quality raw materials. This compound is essential for advancing chemical synthesis in both academic and industrial settings within Indonesia.

  • Synthesis of Heterocyclic Compounds: Methyl Indole-3-carboxylate is ideal for creating indole-based structures, which are common in pharmaceuticals and advanced materials.
  • Organic Reaction Research: Its reactivity and stability make it a valuable reagent in various substitution and ring-opening reactions.
  • Drug Development Studies: The compound's ability to form diverse functional groups supports the synthesis of potential therapeutic agents.
  • Material Science Applications: It is used in the production of polymers and other materials with unique chemical properties.
  • Academic and Industrial Research: Its widespread use in both settings highlights its importance in advancing chemical innovation.

Brand TCI
CAS number 942-24-5
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light

Methyl Indole-3-carboxylate should be stored in a cool, dry place away from direct light to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. As a solid compound, it is typically handled in a well-ventilated laboratory environment to ensure safe working conditions. General laboratory precautions include wearing appropriate personal protective equipment such as gloves and safety goggles. Proper labeling of storage containers is essential to avoid misidentification. This compound should be kept away from incompatible materials to prevent any potential chemical interactions.

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