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CAS 25365-71-3

2-Phenylindole-3-carboxaldehyde TCI P2273

2-Phenylindole-3-carboxaldehyde TCI P2273

Chemical Identity

CAS No.
25365-71-3
PubChem
CID 613305·SID 253661181
Formula
C15H11NO
Molecular weight
221.25 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-phenyl-1H-indole-3-carbaldehyde
SMILES
C1=CC=C(C=C1)C2=C(C3=CC=CC=C3N2)C=O
InChIKey
IFIFXODAHZPTEY-UHFFFAOYSA-N
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2-Phenylindole-3-carboxaldehyde is a chemical compound widely used in organic reactions for the synthesis of complex heterocyclic compounds. It serves as a crucial building block in laboratory settings, enabling the creation of modified indole structures with specific functional groups. This compound is essential for researchers aiming to develop compounds with targeted biological activities. Its unique molecular structure contributes to its versatility in various chemical transformations.

The compound's high reactivity is due to its molecular structure, which includes a carbonyl group at position 3 and an indole ring at position 2. These features make it suitable for reactions such as condensation, substitution, and functional group modifications. Its ability to participate in multiple chemical processes makes it a preferred choice for synthetic chemists. The compound’s reactivity and structural complexity are key factors in its application across different research areas.

In Indonesian laboratories, 2-Phenylindole-3-carboxaldehyde is commonly used in pharmaceutical and material science research. It supports the development of new drugs and advanced materials by providing a foundation for complex molecular structures. Its presence in research facilities enhances the capability to conduct sophisticated chemical syntheses and explore novel chemical properties.

  • Pharmaceutical research utilizes this compound for the synthesis of bioactive molecules due to its structural versatility and reactivity.
  • Organic chemistry experiments benefit from its ability to participate in multiple reaction types, making it ideal for synthetic pathways.
  • Material science studies employ it to create complex molecular frameworks for advanced material development.
  • Drug discovery programs rely on its role in constructing heterocyclic structures with potential therapeutic applications.
  • Academic research institutions use it as a key reagent in the exploration of new chemical reactions and molecular designs.

Brand TCI
CAS number 25365-71-3
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

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize exposure. It is important to keep it away from incompatible substances to ensure safe storage and handling in the laboratory.

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