Methyl 3-Bromo-2-fluorobenzoate TCI M2711

Chemical Identity

CAS No.: 206551-41-9
PubChem: CID 21584505·SID 354333786
Formula: C8H6BrFO2
Molecular weight: 233.03 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3-bromo-2-fluorobenzoate
SMILES: COC(=O)C1=C(C(=CC=C1)Br)F
InChIKey: ZWOFHFOFKBYRHV-UHFFFAOYSA-N

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Methyl 3-Bromo-2-fluorobenzoate is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It plays a crucial role in laboratory settings where researchers are engaged in the development of new compounds, including pharmaceuticals, industrial chemicals, and organic reaction intermediates. This compound is particularly valuable in synthetic chemistry due to its ability to participate in various reaction mechanisms, making it a versatile tool for chemists working on advanced molecular designs. Its presence in laboratory workflows is essential for those aiming to create novel structures with specific functional groups and molecular frameworks.

The compound's unique chemical properties, including its halogen substituents (bromine and fluorine), make it a preferred choice for substitution reactions, electrophilic reactions, and functional group transformations. Its stability under different reaction conditions allows it to be used in both polar and non-polar solvents, enhancing its applicability across a wide range of synthetic strategies. The reactivity and structural complexity of Methyl 3-Bromo-2-fluorobenzoate make it a reliable and efficient reagent for laboratory synthesis, especially in the context of organic chemistry research.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in academic and research institutions. It is a key component in projects related to drug development, material science, and chemical synthesis. Its availability and chemical properties make it a valuable resource for scientists and researchers working on innovative chemical processes and molecular design.

TCI brochures (PDF)

Fluorination Reagents, Fluorinated Building Blocks 2026-03-18 · p. 23

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Organic synthesis projects benefit from this compound due to its reactivity and ability to participate in substitution reactions, making it ideal for creating complex molecular structures.
Pharmaceutical research utilizes this compound as a building block for the development of new drugs, particularly in the synthesis of heterocyclic compounds and functionalized aromatic systems.
Industrial chemical production often incorporates this compound in the creation of specialty chemicals and intermediates for various applications, including polymer science and agrochemicals.
Academic research in chemistry labs uses this compound to explore new synthetic methodologies and reaction mechanisms, supporting both undergraduate and graduate studies.
Environmental chemistry studies may involve this compound in the analysis of halogenated organic pollutants and their behavior in different environmental matrices.

Brand	TCI
CAS number	206551-41-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply formats
Physical form	Solid, crystalline appearance
Storage	Store in a cool, dry place away from direct sunlight and moisture

This compound should be stored in a cool, dry environment to maintain its chemical integrity and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure, which can affect its stability and reactivity. Due to its halogenated nature, it is important to handle it with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is generally stable under normal storage conditions but should be kept away from incompatible materials such as strong bases or oxidizing agents. Proper labeling and storage practices are essential to maintain a safe and efficient laboratory environment.

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