Ethyl 2-Amino-5-methylthiophene-3-carboxylate TCI E1104

Chemical Identity

Other names: 2-Amino-5-methylthiophene-3-carboxylic Acid Ethyl Ester
CAS No.: 4815-32-1
Formula: C8H11NO2S
Molecular weight: 185.24 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: ethyl 2-amino-5-methylthiophene-3-carboxylate
SMILES: CCOC(=O)C1=C(SC(=C1)C)N
InChIKey: AYBUNZGJQVYGTM-UHFFFAOYSA-N
MDL: MDL01922142
PubChem: CID 4062885

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Ethyl 2-Amino-5-methylthiophene-3-carboxylate is a chemical compound widely used in organic synthesis reactions within laboratory settings. As a heterocyclic building block, it plays a crucial role in the development of complex molecular structures. Its unique chemical structure, featuring a thiophene ring with amino and methyl substituents, makes it a versatile intermediate in various synthetic pathways. This compound is particularly valuable for researchers seeking to create biologically active molecules, including pharmaceuticals and pharmacological agents.

The compound's chemical stability and reactivity make it a preferred choice for laboratory applications. Its polar nature allows it to dissolve in organic solvents such as ethyl acetate and acetone, facilitating its use in diverse reaction conditions. The presence of both amino and methyl groups enhances its reactivity, enabling participation in a wide range of chemical modifications. Additionally, its relatively low toxicity ensures safer handling in laboratory environments, reducing potential risks for researchers.

In Indonesian laboratories, this compound is commonly utilized in pharmacological, organic chemistry, and biochemical research. Local researchers frequently employ it in the synthesis of bioactive compounds and the study of molecular interactions. Its availability through suppliers like AMI Scientific ensures that it remains a key component in the toolkit of Indonesian scientists working in these fields.

Organic synthesis applications benefit from this compound's reactivity and structural versatility, enabling the creation of complex molecules.
Pharmacological research utilizes it as a building block for developing new drugs and bioactive compounds.
Biochemical studies often incorporate this compound to investigate molecular interactions and biological activity.
Heterocyclic compound synthesis relies on its unique thiophene ring structure for constructing diverse chemical frameworks.
Chemical modification experiments take advantage of its amino and methyl groups for functional group transformations.

Brand	TCI
CAS number	4815-32-1
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid or crystalline, depending on the batch
Storage	Store in a cool, dry place away from direct sunlight

This compound 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 moisture absorption and maintain its chemical integrity. Due to its polar nature, it is advisable to handle it in a well-ventilated area to minimize exposure. While it has relatively low toxicity, standard laboratory safety protocols should still be followed, including the use of personal protective equipment. Proper labeling of containers is essential to ensure safe handling and prevent accidental contamination. Its stability under normal storage conditions makes it suitable for long-term use in laboratory settings.

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