Methyl 3-Bromothiophene-2-carboxylate TCI M2590

Chemical Identity

CAS No.: 26137-08-6
PubChem: CID 2740074·SID 253662198
Formula: C6H5BrO2S
Molecular weight: 221.07 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3-bromothiophene-2-carboxylate
SMILES: COC(=O)C1=C(C=CS1)Br
InChIKey: PEGSJNCGPSIJOX-UHFFFAOYSA-N

Rp 1.458.450,00

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Berat 1g 5g

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Methyl 3-Bromothiophene-2-carboxylate is a chemical compound widely used in organic synthesis reactions, particularly in the formation of heterocyclic compounds. As a building block, it plays a crucial role in the development of complex molecular structures within laboratory settings. This compound is essential for researchers working in organic chemistry, pharmaceuticals, and advanced material science. Its versatility allows it to participate in various reactions such as substitution, coupling, and electrophilic reactions, making it a valuable tool for synthetic chemists.

The compound's chemical properties, including the presence of bromo and carboxylate groups, make it a preferred choice for synthetic applications. These functional groups enable controlled reactivity and compatibility with a range of reaction conditions. Its molecular structure is stable, yet reactive enough to facilitate the formation of new chemical bonds. This balance of stability and reactivity ensures that it can be effectively utilized in multiple experimental setups without compromising the integrity of the final product.

In Indonesian laboratories, Methyl 3-Bromothiophene-2-carboxylate is commonly used in scientific research related to pharmaceutical compounds, organic materials, and the development of new chemical entities. Its availability supports researchers in conducting experiments that require reactive and specific chemical intermediates. The compound's role in these studies highlights its importance in advancing scientific knowledge and innovation in the region.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 4

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive bromo and carboxylate functional groups.
Pharmaceutical research for the development of new drug molecules and bioactive compounds.
Material science applications in the creation of advanced organic materials and polymers.
Academic research in chemical reactivity and molecular structure modification.
Industrial chemical processes requiring stable and versatile building blocks for complex molecule synthesis.

Brand	TCI
CAS number	26137-08-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid or liquid, depending on supplier packaging
Storage	—

Methyl 3-Bromothiophene-2-carboxylate should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Storage in a fume hood is advisable when working with volatile or reactive substances. The compound should not be exposed to incompatible materials, such as strong acids or bases, to maintain its stability and ensure safe laboratory practices.

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