Methyl 3-Hydroxy-2-thiophenecarboxylate TCI M2716

Chemical Identity

CAS No.: 5118-06-9
PubChem: CID 581127·SID 354333948
Formula: C6H6O3S
Molecular weight: 158.18 g/mol
Purity: >97.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 3-hydroxythiophene-2-carboxylate
SMILES: COC(=O)C1=C(C=CS1)O
InChIKey: SEMVRXMFCHXUMD-UHFFFAOYSA-N

Rp 1.035.300,00

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Methyl 3-Hydroxy-2-thiophenecarboxylate is a chemical compound widely used in organic reactions for the synthesis of heterocyclic compounds. This material plays a crucial role in laboratory settings, particularly in research involving the construction of complex molecular structures. Its unique chemical structure, which includes a thiophene ring and a carboxylate group attached to an oxygen atom, makes it a valuable building block in various synthetic pathways. Due to its reactivity, it is often employed in the development of compounds with biological activity, such as pharmaceuticals and industrial chemicals.

The compound is known for its high reactivity, especially at the hydroxyl and carboxylate positions, allowing it to participate in a variety of chemical reactions. This reactivity makes it a preferred choice for chemists seeking to modify molecular structures with precision. It is compatible with a wide range of reagents, including acids, bases, and organic solvents, which enhances its versatility in synthetic applications. Its ability to undergo substitution, coupling, and structural modification reactions makes it an essential component in many organic synthesis protocols.

In Indonesian laboratories, Methyl 3-Hydroxy-2-thiophenecarboxylate is commonly used in organic chemistry research, particularly in the synthesis of pharmacological compounds and industrial chemicals. Its role in creating complex molecular structures is vital for advancing research in both academic and industrial settings. The compound is frequently utilized in studies aimed at developing new drugs and chemical materials, contributing to the growth of scientific innovation in the region.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 9

Related TCI products

Organic synthesis of heterocyclic compounds due to its reactive thiophene ring and carboxylate group.
Development of pharmaceuticals and industrial chemicals through structural modification and substitution reactions.
Research in pharmacological compound synthesis, leveraging its ability to participate in various chemical transformations.
Creation of complex molecular structures for advanced chemical research and material development.
Use in academic and industrial laboratories for the production of bioactive compounds and specialty chemicals.

Brand	TCI
CAS number	5118-06-9
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Solid or liquid, depending on the specific product variant
Storage	Store in a cool, dry place away from direct sunlight and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to strong acids or bases to prevent unwanted chemical reactions. Proper ventilation is essential when working with this material to ensure a safe laboratory environment. Always follow standard laboratory safety protocols when handling reactive chemicals.

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