2-Bromoethyl Benzoate TCI B0065

Chemical Identity

CAS No.: 939-54-8
PubChem: CID 523090·SID 87563267
Formula: C9H9BrO2
Molecular weight: 229.07 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromoethyl benzoate
SMILES: C1=CC=C(C=C1)C(=O)OCCBr
InChIKey: KNBBDZULQFKSIE-UHFFFAOYSA-N

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2-Bromoethyl Benzoate is a chemical compound widely used as a building block in the synthesis of complex organic compounds. It serves as a key reagent in various chemical reactions, particularly those involving bromo substitution on alkyl chains. This compound is essential for the development of aromatic and heterocyclic compounds, making it a valuable asset in both academic and industrial research settings. Its versatility and reactivity make it a preferred choice for chemists working on synthetic pathways that require controlled substitution reactions.

The compound's molecular structure is stable, allowing it to react efficiently with a variety of reagents. It exhibits good solubility in organic solvents such as ethyl acetate and chloroform, which facilitates its use in reactions like esterification, hydrolysis, and nucleophilic substitution. The presence of the bromo group enhances its reactivity, enabling it to participate in substitution and radical reactions. These properties make it a reliable and effective material for synthetic chemistry applications.

In Indonesian laboratories, 2-Bromoethyl Benzoate is commonly used in organic chemistry research, particularly in higher education institutions and research centers. It is an essential component in projects focused on the synthesis of new compounds and the study of reaction mechanisms. Its availability and chemical properties make it a standard reagent in both teaching and research laboratories across Indonesia.

Related TCI products

Organic synthesis applications benefit from 2-Bromoethyl Benzoate due to its reactivity and ability to undergo substitution reactions, making it ideal for creating complex molecular structures.
It is frequently used in nucleophilic substitution reactions because of its bromo group, which facilitates the formation of new carbon-carbon bonds in synthetic pathways.
The compound's solubility in organic solvents like ethyl acetate and chloroform makes it suitable for esterification and hydrolysis reactions in laboratory settings.
It supports research in heterocyclic compound synthesis, where controlled substitution reactions are essential for the development of pharmaceutical and industrial chemicals.
In academic laboratories, it is used as a teaching tool to demonstrate reaction mechanisms and synthetic strategies in organic chemistry courses.

Brand	TCI
CAS number	939-54-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

2-Bromoethyl Benzoate should be stored in a cool, dry location, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent exposure to air and moisture. Due to its reactive nature, it should be stored separately from strong oxidizing agents and incompatible substances. In laboratory settings, proper ventilation is essential when handling this compound to ensure safe working conditions. Always use appropriate personal protective equipment, including gloves and safety goggles, to minimize exposure. Regular inspection of storage containers is advised to maintain the integrity and safety of the material.

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