N-(Bromomethyl)phthalimide TCI P1192

Chemical Identity

CAS No.: 5332-26-3
PubChem: CID 79244·SID 87575291
Formula: C9H6BrNO2
Molecular weight: 240.05 g/mol
Purity: >96.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(bromomethyl)isoindole-1,3-dione
SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)CBr
InChIKey: UUSLLECLCKTJQF-UHFFFAOYSA-N

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N-(Bromomethyl)phthalimide is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and phthalimide derivatives. It serves as a key building block in the creation of complex molecular structures, including pharmaceuticals, industrial chemicals, and food additives. In laboratory settings, this compound plays a crucial role in nucleophilic substitution and coupling reactions, enabling the formation of new molecular bonds. Its versatility makes it an essential tool for researchers working in both academic and industrial environments.

The chemical stability and reactivity of N-(Bromomethyl)phthalimide make it a preferred choice for various synthetic applications. The presence of a bromo group and the phthalimide ring allows it to participate in substitution and electrophilic reactions, offering a wide range of synthetic possibilities. These properties make it ideal for use in organic chemistry and pharmacological research, where precise control over molecular structures is essential. Its reliability and consistent performance contribute to its popularity among chemists.

In Indonesian laboratories, N-(Bromomethyl)phthalimide is commonly used in organic chemistry research, especially in higher education institutions and research centers. It is a fundamental component in the synthesis of complex molecules, supporting both teaching and research activities. Its availability and effectiveness make it a standard reagent in many laboratory workflows, facilitating the development of new compounds and materials.

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive bromomethyl group and phthalimide ring.
Nucleophilic substitution reactions where it acts as a versatile electrophilic substrate for functional group transformation.
Coupling reactions in the formation of complex molecular architectures, particularly in pharmaceutical research.
Development of industrial chemicals and food additives through controlled chemical modifications.
Educational and research applications in Indonesian universities and research institutes for advanced chemical studies.

Brand	TCI
CAS number	5332-26-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid (as per standard chemical properties)
Storage	Store in a cool, dry place away from light and moisture

N-(Bromomethyl)phthalimide should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid contact with incompatible substances, and ensure proper ventilation when working with this compound. Regular monitoring of storage conditions is advised to maintain its integrity and effectiveness in laboratory applications.

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