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Catalog Number:
42687
CAS Number:
4506-71-2
2-amino-4,5,6,7-tétrahydrobenzo[ b ]thiophène-3-carboxylate d'éthyle
Purity:
≥ 98 % (dosage par titration)
Synonym(s):
2-Amino-3-carbéthoxy-4,5-tétraméthylènethiophène, 2-Amino-3-éthoxycarbonyl-4,5-tétraméthylènethiophène, Ester éthylique de l'acide 2-amino-4,5,6,7-tétrahydrobenzo[b]thiophène-3-carboxylique
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Informations sur le produit

Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate is a versatile compound recognized for its unique structure and potential applications in medicinal chemistry and organic synthesis. This compound features a benzothiophene core, which is known for its biological activity, making it a valuable candidate in the development of pharmaceuticals. Its amino and carboxylate functional groups enhance its reactivity, allowing for various modifications that can lead to the synthesis of novel derivatives with improved efficacy. Researchers have explored its use in the synthesis of bioactive molecules, particularly in the field of drug discovery, where it may serve as a scaffold for creating new therapeutic agents.

In addition to its applications in drug development, Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate can be utilized in the production of agrochemicals and dyes, showcasing its versatility across different industries. Its unique properties, such as solubility and stability, make it an attractive option for formulation in various applications. As the demand for innovative compounds continues to rise, this chemical stands out for its potential to contribute significantly to advancements in both pharmaceutical and agricultural sectors.

Numéro CAS 
4506-71-2
Formule moléculaire
C 11 H 15 NO 2 S
Poids moléculaire 
225.31
Point de fusion 
114 - 117 °C
Informations générales
Numéro CAS 
4506-71-2
Formule moléculaire
C 11 H 15 NO 2 S
Poids moléculaire 
225.31
Point de fusion 
114 - 117 °C
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Ethyl 2-amino-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly those targeting neurological disorders, due to its ability to interact with specific neurotransmitter systems.
  • Biochemical Research: It is used in studies exploring the mechanisms of enzyme inhibition, providing insights into metabolic pathways and potential therapeutic targets.
  • Material Science: The compound is investigated for its properties in developing novel materials, such as conductive polymers, which can be applied in electronics and energy storage devices.
  • Agricultural Chemistry: Researchers are exploring its potential as a bioactive compound in agrochemicals, aiming to enhance crop protection and yield through its unique biological activity.
  • Natural Product Synthesis: It is employed in the synthesis of complex natural products, facilitating the development of new compounds with potential medicinal properties.

Citations