Ethyl 2-Bromopropionate TCI B0646

Chemical Identity

CAS No.: 535-11-5
PubChem: CID 79040·SID 87563653
Formula: C5H9BrO2
Molecular weight: 181.03 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 2-bromopropanoate
SMILES: CCOC(=O)C(C)Br
InChIKey: ARFLASKVLJTEJD-UHFFFAOYSA-N

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Ethyl 2-Bromopropionate is a chemical compound widely used as a building block in organic synthesis. It serves as a key intermediate in various chemical reactions, particularly those involving nucleophilic substitution or electrophilic reactions. In laboratory settings, this compound plays a crucial role in the development of complex organic molecules, including esters, halides, and heterocyclic compounds. Its versatility makes it an essential tool for chemists working on synthetic pathways that require bromide substitution or functional group modification.

The chemical properties of Ethyl 2-Bromopropionate make it a preferred choice for synthetic chemists. It exhibits stability under certain conditions, yet remains highly reactive in nucleophilic substitution reactions. This reactivity allows it to participate effectively in a wide range of chemical transformations, making it a valuable reagent in both academic and industrial research. Its ability to undergo substitution reactions with various nucleophiles further enhances its utility in the synthesis of diverse organic compounds.

In Indonesian laboratories, Ethyl 2-Bromopropionate is commonly used in organic chemistry research, especially in academic institutions and research centers. Its availability in multiple packaging sizes ensures convenience for both small-scale experiments and larger laboratory operations. The compound’s role in synthesizing esters and halides makes it a sought-after material for researchers aiming to explore new chemical structures and reactions.

TCI brochures (PDF)

Biomaterials Research Reagents 2025-02-19 · p. 29

Related TCI products

Nucleophilic Substitution Reactions: Ethyl 2-Bromopropionate is ideal for reactions where bromide substitution is required, offering reliable results in synthetic pathways.
Ester Synthesis: This compound serves as a precursor for ester formation, making it a key reagent in the synthesis of organic compounds.
Halide Compound Development: Its reactivity allows it to be used in the creation of halide derivatives, which are essential in organic chemistry research.
Structural Modification Studies: It is widely used in experiments aimed at modifying molecular structures, particularly in heterocyclic compound synthesis.
Reactivity Testing: Ethyl 2-Bromopropionate is frequently employed in testing the reactivity of different nucleophiles in controlled laboratory conditions.

Brand	TCI
CAS number	535-11-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various sizes to suit different laboratory needs
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

Ethyl 2-Bromopropionate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its chemical stability. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation to minimize inhalation risks. The compound should not be stored near incompatible materials such as strong bases or oxidizing agents. Always follow standard safety protocols when working with reactive chemicals to maintain a safe laboratory environment.

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