N-(6-Bromohexyl)phthalimide TCI B4987

Chemical Identity

CAS No.: 24566-79-8
PubChem: CID 141120·SID 354333707
Formula: C14H16BrNO2
Molecular weight: 310.19 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(6-bromohexyl)isoindole-1,3-dione
SMILES: C1=CC=C2C(=C1)C(=O)N(C2=O)CCCCCCBr
InChIKey: OAZFTIPKNPTDIO-UHFFFAOYSA-N

Rp 2.969.400,00

~~Rp 2.091.600,00~~ Rp 2.969.400,00

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N-(6-Bromohexyl)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 reagent for various synthetic pathways. This compound is particularly valuable for its ability to participate in substitution and coupling reactions, making it an essential tool for researchers working on the development of new chemical structures. Its presence in the category of non-heterocyclic building blocks highlights its utility in creating a wide range of organic compounds.

The chemical properties of N-(6-Bromohexyl)phthalimide make it a preferred choice in laboratory settings. It exhibits stability under normal conditions and can react with a variety of reagents such as amines, acids, and alkali metals. The presence of a bromo group at the sixth position of the alkyl chain enhances its reactivity, making it suitable for high-activity reactions. Its ability to dissolve in organic solvents further improves its practicality for use in diverse experimental setups.

In Indonesian laboratories, N-(6-Bromohexyl)phthalimide is commonly utilized in organic chemistry research, particularly in academic and research institutions. It supports the development of new compounds and is frequently employed in projects involving synthetic chemistry. Its availability and functional versatility make it a reliable choice for both educational and industrial research applications.

Related TCI products

Organic synthesis applications benefit from N-(6-Bromohexyl)phthalimide due to its reactivity and ability to participate in substitution reactions.
It is ideal for coupling reactions where the bromoalkyl group serves as a functional handle for further modifications.
In the development of heterocyclic compounds, this material provides a stable starting point for complex molecular architectures.
It is commonly used in research involving functional group transformations, offering versatility in synthetic strategies.
Indonesian research institutions rely on this compound for advanced chemical studies, supporting both academic and industrial innovation.

Brand	TCI
CAS number	24566-79-8
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 moisture and direct sunlight

N-(6-Bromohexyl)phthalimide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the material in a sealed container to prevent exposure to moisture and air. Due to its bromoalkyl functional group, it is advisable to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It should be stored away from incompatible materials like strong bases or oxidizing agents. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. Regular inspection of storage conditions is necessary to maintain the integrity of the compound throughout its shelf life.

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