Ethyl 2-Amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate TCI A1355

Chemical Identity

CAS No.: 4506-71-2
PubChem: CID 78262·SID 87562811
Formula: C11H15NO2S
Molecular weight: 225.31 g/mol
Purity: >98.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylate
SMILES: CCOC(=O)C1=C(SC2=C1CCCC2)N
InChIKey: CDYVTVLXEWMCHU-UHFFFAOYSA-N

Rp 3.153.150,00

~~Rp 2.220.750,00~~ Rp 3.153.150,00

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Ethyl 2-Amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate is a chemical compound widely used in organic synthesis reactions within laboratory settings. This compound is a heterocyclic building block, which makes it essential for the development of complex molecular structures. Its unique chemical structure enables it to participate in various synthetic pathways, making it a valuable tool for researchers in both academic and industrial environments. Due to its versatility, it is frequently employed in the synthesis of bioactive compounds, contributing to advancements in pharmaceutical and chemical research.

The compound is characterized by the presence of both amino and carboxylate functional groups, which significantly enhance its reactivity in chemical reactions. These groups allow it to undergo a variety of transformations, such as acylation, amidation, and coupling reactions. The heterocyclic framework also provides structural stability, which is crucial for maintaining the integrity of the molecule during synthesis. This combination of reactivity and stability makes it a preferred choice for chemists seeking to design and synthesize new compounds with specific functional properties.

In Indonesian laboratories, this compound is commonly used in scientific research and pharmaceutical development. With the growing sophistication of laboratory facilities, the demand for such specialized reagents has increased. Its ability to participate in precise and controlled chemical reactions makes it an essential component in the synthesis of bioactive molecules. Its role in the development of new drugs and chemical compounds underscores its importance in modern laboratory practices.

TCI brochures (PDF)

Thiophenes 2026-06-29 · p. 13

Related TCI products

Organic synthesis of bioactive compounds due to its reactivity and functional group versatility.
Development of pharmaceuticals as a building block for complex molecular structures.
Research in medicinal chemistry for the creation of novel drug candidates.
Synthesis of heterocyclic derivatives for applications in medicinal and agricultural chemistry.
Use in academic research for teaching and experimental purposes in chemical synthesis.

Brand	TCI
CAS number	4506-71-2
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 supplier packaging
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Proper labeling of containers is essential for safe handling and identification. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. Due to its reactivity, it should be stored separately from strong oxidizing or reducing agents. Regular monitoring of storage conditions is advised to ensure optimal preservation of the compound.

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