Ethyl (4-Bromobenzoyl)acetate TCI E1117

Chemical Identity

Other names: (4-Bromobenzoyl)acetic Acid Ethyl Ester · Ethyl 3-(4-Bromophenyl)-3-oxopropionate · 3-(4-Bromophenyl)-3-oxopropionic Acid Ethyl Ester
CAS No.: 26510-95-2
PubChem: CID 2757149·SID 354333429
Formula: C11H11BrO3
Molecular weight: 271.11 g/mol
Purity: >98.0%(GC)
Storage: 0-10°C
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 3-(4-bromophenyl)-3-oxopropanoate
SMILES: CCOC(=O)CC(=O)C1=CC=C(C=C1)Br
InChIKey: PBDYXCKRDRCJDC-UHFFFAOYSA-N
MDL: MDL00231243

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Ethyl (4-Bromobenzoyl)acetate is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It serves as an essential reagent in laboratory settings, particularly in organic chemistry research. Its molecular structure, featuring a bromobenzoate group and an ethyl group, makes it highly versatile for various chemical reactions, including esterification and substitution. This compound plays a crucial role in the development of new chemical entities, especially in pharmaceutical and industrial chemistry.

The compound's chemical properties make it a preferred choice for laboratory applications. It exhibits stability under certain conditions but is highly reactive in specific chemical reactions such as hydrolysis and nucleophilic substitution. The presence of a bromo group, which is strongly electron-withdrawing, enhances its reactivity in aromatic substitution reactions. Its high purity and solid form ensure consistent performance in synthetic processes, making it a reliable material for researchers.

In Indonesian laboratories, Ethyl (4-Bromobenzoyl)acetate is commonly used in research and development projects, particularly in the fields of pharmacy and organic chemistry. It is a key component in the synthesis of new compounds and is frequently utilized by researchers in educational and research institutions. Its availability and chemical properties make it a valuable resource for advancing scientific studies in the region.

Related TCI products

Organic synthesis applications benefit from Ethyl (4-Bromobenzoyl)acetate due to its reactivity in esterification and substitution reactions, enabling the creation of complex molecular structures.
Pharmaceutical research utilizes this compound as a building block for developing new drug molecules, leveraging its bromo group for targeted chemical modifications.
Industrial chemical synthesis relies on this material for the production of specialty chemicals, as its stability and reactivity support efficient reaction pathways.
Academic research institutions use it in teaching and experimental setups to demonstrate key organic reaction mechanisms and synthetic strategies.
Chemical innovation projects integrate this compound into novel synthetic routes, enhancing the versatility of laboratory workflows in research and development.

Brand	TCI
CAS number	26510-95-2
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

Ethyl (4-Bromobenzoyl)acetate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong bases or acids. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications. Proper labeling and safe handling practices are essential to ensure the safety of laboratory personnel and the effectiveness of the compound in chemical processes.

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