5-(2-Bromoethyl)-2,3-dihydrobenzofuran TCI B4066

Chemical Identity

CAS No.: 127264-14-6
PubChem: CID 21831160·SID 253659632
Formula: C10H11BrO
Molecular weight: 227.10 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 5-(2-bromoethyl)-2,3-dihydro-1-benzofuran
SMILES: C1COC2=C1C=C(C=C2)CCBr
InChIKey: JRKZQRRYNCMSCB-UHFFFAOYSA-N

Rp 2.650.200,00

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5-(2-Bromoethyl)-2,3-dihydrobenzofuran is a chemical compound widely used in organic reactions for the synthesis of complex heterocyclic compounds. As a building block in chemical research, it serves as a fundamental component in the development of new molecular structures. This compound is particularly valuable in laboratory settings where the creation of intricate chemical frameworks is required. Its unique molecular structure, featuring a bromoethyl group and a benzofuran ring, makes it a versatile reagent in synthetic chemistry.

The compound’s high reactivity and the presence of the bromo group make it a preferred choice for nucleophilic substitution reactions and coupling reactions. Its ability to participate in various reaction mechanisms allows chemists to design and synthesize a wide range of functional molecules. The bromoethyl substitution enhances its utility in synthetic pathways, offering multiple reaction sites for further modification. These properties make it an essential tool in both academic and industrial research environments.

In Indonesian laboratories, this compound is commonly used by researchers and educational institutions for organic chemistry studies, new compound development, and molecular structure analysis. Its role in creating complex chemical structures is critical for advancing research in pharmaceuticals, industrial chemicals, and functional materials. The demand for such reactive and structurally diverse compounds continues to grow, making it a key reagent in modern chemical synthesis.

Related TCI products

Organic synthesis of complex heterocyclic compounds due to its reactive bromoethyl group and benzofuran ring.
Nucleophilic substitution reactions as a good substrate for substitution at the bromoethyl position.
Coupling reactions to form new carbon-carbon bonds in the development of functional molecules.
Structural studies of molecular frameworks in academic and industrial research settings.
Development of pharmaceuticals and industrial chemicals through synthetic pathways involving this compound.

Brand	TCI
CAS number	127264-14-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities as per supplier specifications
Physical form	Solid or liquid, depending on supplier packaging
Storage	Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers to prevent exposure to moisture and air, which may affect its stability. Due to its bromoethyl group, it may react with certain substances, so it should be kept separate from strong bases, oxidizing agents, and other reactive materials. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling. In laboratory settings, it is important to ensure good ventilation and to follow standard chemical safety protocols to minimize risks.

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