N-Bromophthalimide TCI B1697

Chemical Identity

CAS No.: 2439-85-2
PubChem: CID 75542·SID 87564597
Formula: C8H4BrNO2
Molecular weight: 226.03 g/mol
Purity: >95.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromoisoindole-1,3-dione
SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)Br
InChIKey: MARXMDRWROUXMD-UHFFFAOYSA-N

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N-Bromophthalimide is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and complex molecular structures. As a key reagent in chemical laboratories, it serves as a building block for substitution reactions and radical processes. Its unique chemical structure makes it highly reactive under various conditions, enabling it to participate in a wide range of synthetic pathways. This compound is especially valuable in the development of new organic compounds due to its ability to undergo selective transformations.

One of the main reasons N-Bromophthalimide is preferred is its high reactivity and stability under controlled laboratory conditions. The presence of bromine in its molecular structure makes it an ideal candidate for halogen substitution reactions. It is also compatible with a variety of reagents and solvents, enhancing its versatility in different synthetic strategies. Its chemical stability ensures that it maintains its properties over time, making it a reliable choice for both research and educational purposes.

In Indonesian laboratories, N-Bromophthalimide is commonly used in organic chemistry research, especially in universities and research institutions focused on compound synthesis. It is also incorporated into chemistry education to demonstrate reactivity and reaction mechanisms. Its role in both academic and industrial settings highlights its importance as a fundamental chemical reagent.

TCI brochures (PDF)

Halogenation Reagents 2026-04-03 · p. 7

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactivity and halogen substitution capabilities.
Radical reaction studies as it participates in free radical mechanisms under controlled conditions.
Teaching demonstrations in chemistry courses to illustrate reactivity and reaction pathways.
Development of complex molecular structures in research laboratories through substitution reactions.
Preparation of halogenated derivatives for further chemical modifications and applications.

Brand	TCI
CAS number	2439-85-2
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid powder
Storage	Store in a cool, dry place away from light and moisture

N-Bromophthalimide should be stored in a cool, dry place, away from light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Avoid contact with incompatible materials such as strong bases or reducing agents. Proper labeling and storage conditions help ensure the safety and effectiveness of the compound in laboratory settings.

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