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CAS 4651-81-4

Methyl 2-Aminothiophene-3-carboxylate TCI M1697

Methyl 2-Aminothiophene-3-carboxylate TCI M1697

Chemical Identity

CAS No.
4651-81-4
Purity
>98.0%(GC)(T)
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Methyl 2-Aminothiophene-3-carboxylate is a chemical compound widely used in organic synthesis reactions. It belongs to the category of heterocyclic building blocks, making it a valuable tool in the laboratory for creating complex molecular structures. This compound is often employed as a starting material in the synthesis of various pharmaceuticals, industrial chemicals, and bioactive compounds. Its role as a fundamental building block allows researchers to design and develop new compounds with specific functional groups and molecular frameworks.

The compound's chemical properties, including its heterocyclic structure containing sulfur and nitrogen atoms, make it highly reactive in substitution and condensation reactions. These characteristics enable it to participate in a wide range of synthetic pathways, offering versatility in chemical transformations. Its stability under certain conditions further enhances its utility in controlled laboratory environments. The presence of both nitrogen and sulfur atoms also makes it an attractive candidate for reactions involving the formation of heterocyclic bonds.

In Indonesian laboratories, Methyl 2-Aminothiophene-3-carboxylate is extensively used in organic chemistry research, particularly in pharmacology and the synthesis of bioactive compounds. It is a key component in the development of new drugs and chemical products. Many research institutions and universities rely on this compound for its reliability and effectiveness in complex chemical processes. Its application is widespread in both academic and industrial research settings.

  • Organic synthesis applications benefit from its reactivity and heterocyclic structure, enabling the creation of complex molecules.
  • Pharmaceutical research utilizes it as a building block for synthesizing bioactive compounds and drug candidates.
  • Industrial chemical development leverages its versatility in forming diverse molecular frameworks.
  • Bioactive compound synthesis relies on its ability to participate in precise and controlled chemical reactions.
  • Academic research in pharmacology and medicinal chemistry frequently employs it for compound development and structural modifications.

Brand TCI
CAS number 4651-81-4
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid powder
Storage Store in a cool, dry place away from direct sunlight

Methyl 2-Aminothiophene-3-carboxylate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Suitable storage conditions include a controlled temperature range between 15°C and 25°C. Avoid exposure to direct sunlight and high humidity to ensure long-term integrity. When handling, use appropriate personal protective equipment such as gloves and safety goggles to minimize direct contact. This compound is generally non-hazardous under normal laboratory conditions but should be treated with care to maintain safety standards.

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