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TCI

CAS 7386-21-2

N-(4-Chlorophenyl)phthalimide TCI C1958

N-(4-Chlorophenyl)phthalimide TCI C1958

Chemical Identity

CAS No.
7386-21-2
PubChem
CID 81867·SID 87558292
Formula
C14H8ClNO2
Molecular weight
257.67 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(4-chlorophenyl)isoindole-1,3-dione
SMILES
C1=CC=C2C(=C1)C(=O)N(C2=O)C3=CC=C(C=C3)Cl
InChIKey
QKHKQJWODBAIMN-UHFFFAOYSA-N
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N-(4-Chlorophenyl)phthalimide is a chemical compound widely used as a building block in the synthesis of complex molecules. It plays a crucial role in organic chemistry laboratories, where it serves as a versatile intermediate in various chemical reactions. This compound is particularly valuable for its ability to participate in reactions involving carbon-nitrogen bond formation, making it a key component in the development of new chemical entities. Its importance extends across multiple research fields, including pharmaceuticals and materials science, where it contributes to the creation of novel compounds with specific functional properties.

The compound is known for its stable molecular structure and relatively high reactivity, which allows it to readily engage in substitution and condensation reactions. These characteristics make it an ideal candidate for a wide range of synthetic applications. Its chemical properties can be tailored to meet specific research needs, enabling chemists to design and synthesize complex molecules with desired functionalities. This adaptability enhances its utility in both fundamental and applied research settings.

In Indonesian laboratories, N-(4-Chlorophenyl)phthalimide is extensively used in pure and applied chemical research. It is commonly employed in the synthesis of new organic compounds, drug development, and studies on organic reactivity. Its presence in academic and industrial research institutions underscores its significance as a fundamental reagent in modern chemical investigations.

  • Organic synthesis of complex heterocyclic compounds due to its ability to form stable carbon-nitrogen bonds.
  • Development of new pharmaceuticals through modification of aromatic compounds and functional group introduction.
  • Investigation of organic reactivity in academic research settings for understanding reaction mechanisms.
  • Preparation of intermediates for the synthesis of advanced materials with specific chemical properties.
  • Support for drug discovery programs by enabling the creation of structurally diverse compounds for biological testing.

Brand TCI
CAS number 7386-21-2
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

N-(4-Chlorophenyl)phthalimide should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Due to its chemical nature, it should be stored separately from incompatible substances to avoid any potential reactions. Regular monitoring of storage conditions is essential to ensure the compound remains in optimal condition for use in research applications.

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