N-(2-Bromoethyl)phthalimide TCI B0597

Chemical Identity

CAS No.: 574-98-1
PubChem: CID 11325·SID 87563612
Formula: C10H8BrNO2
Molecular weight: 254.08 g/mol
Purity: >98.0%(GC)(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(2-bromoethyl)isoindole-1,3-dione
SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)CCBr
InChIKey: CHZXTOCAICMPQR-UHFFFAOYSA-N

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N-(2-Bromoethyl)phthalimide is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It plays a crucial role in laboratory settings where organic chemists aim to create molecules with specific functional groups or structural features. This compound is particularly valuable for its versatility in undergoing substitution and electrophilic reactions, making it a key component in the development of heterocyclic and complex molecular structures. Its presence in various synthetic pathways highlights its importance in both academic and industrial research environments.

The compound's stable chemical structure and controlled reactivity make it a preferred choice for researchers seeking reliable and predictable outcomes in their experiments. Its ability to participate in a range of chemical reactions, including those involving free radicals, enhances its utility in diverse synthetic strategies. The high purity and consistent quality of N-(2-Bromoethyl)phthalimide ensure that it meets the rigorous demands of scientific research, especially in fields requiring precision and accuracy. These properties contribute to its widespread use in both basic and applied research.

In Indonesian laboratories, N-(2-Bromoethyl)phthalimide is frequently utilized by researchers and students working in organic chemistry and pharmaceutical sciences. Its availability and reliable quality make it an essential reagent for those engaged in synthetic chemistry, drug development, and material science. The compound's role in supporting scientific innovation underscores its significance in the Indonesian research community.

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Organic synthesis applications benefit from its reactivity and versatility in forming complex molecular structures.
Pharmaceutical research utilizes it for the development of new drugs and bioactive compounds.
Material science experiments leverage its properties to create advanced chemical materials.
Educational institutions use it as a teaching tool for students learning synthetic chemistry techniques.
Industrial research employs it for the production of specialty chemicals and functional compounds.

Brand	TCI
CAS number	574-98-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-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 light and moisture

N-(2-Bromoethyl)phthalimide should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its quality. In laboratory settings, it should be handled with appropriate personal protective equipment to ensure safety. The compound is generally non-hazardous under normal conditions but should be stored separately from incompatible substances. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications. Proper labeling and secure storage are essential to prevent accidental contamination or misuse.

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