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TCI

CAS 29753-26-2

N-(4-Aminophenyl)maleimide TCI A0825

N-(4-Aminophenyl)maleimide TCI A0825

Chemical Identity

CAS No.
29753-26-2
PubChem
CID 122469·SID 87562348
Formula
C10H8N2O2
Molecular weight
188.18 g/mol
Purity
>93.0%(T)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1-(4-aminophenyl)pyrrole-2,5-dione
SMILES
C1=CC(=CC=C1N)N2C(=O)C=CC2=O
InChIKey
XOPCHXSYQHXLHJ-UHFFFAOYSA-N
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N-(4-Aminophenyl)maleimide is a versatile chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds and complex molecules. As a key building block in organic chemistry, it serves as a crucial intermediate in the formation of maleimide-based structures, which are essential in various scientific applications. This compound is particularly valuable in research areas that require the creation of stable and specific chemical bonds between amino groups and cyclic frameworks. Its role in enabling precise chemical reactions makes it indispensable in modern synthetic chemistry.

The reactivity of N-(4-Aminophenyl)maleimide is one of its defining characteristics, making it a preferred choice for chemists. It exhibits high reactivity towards electrophilic compounds, allowing for a wide range of substitution and addition reactions. This reactivity, combined with its complex molecular structure, enables the synthesis of compounds with specific functional groups and desired properties. Its ability to participate in multiple reaction pathways enhances its utility in the development of pharmaceuticals, materials science, and other advanced chemical applications.

In Indonesian laboratories, N-(4-Aminophenyl)maleimide is extensively used in organic chemistry research, particularly in academic and research institutions. It is a fundamental component in experiments involving the synthesis of heterocyclic compounds, which are vital in drug development and material innovation. Its availability and reliability make it a standard reagent in many chemical laboratories across Indonesia.

TCI brochures (PDF)

  • Organic synthesis of heterocyclic compounds due to its ability to form stable maleimide structures.
  • Development of pharmaceuticals as a key intermediate in the synthesis of bioactive molecules.
  • Creation of advanced materials through chemical reactions that require precise molecular bonding.
  • Research in material science for the production of polymers and functional materials.
  • Academic teaching and experimental research in chemistry laboratories for student and researcher use.

Brand TCI
CAS number 29753-26-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from moisture and direct sunlight

N-(4-Aminophenyl)maleimide should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn when working with it. Avoid contact with skin and eyes, and ensure that spillage is promptly cleaned up using suitable safety procedures. Proper storage and handling are essential to ensure the compound's effectiveness and safety in laboratory applications.

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