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Catalog Number:
19158
CAS Number:
146137-92-0
Ester méthylique de l'acide 5-(trifluorométhyl)benzo[ b ]thiophène-2-carboxylique
Purity:
≥ 96%
Synonym(s):
5-(trifluorométhyl)benzo[ b ]thiophène-2-carboxylate de méthyle
Documents
$103.56 /250 mg
Taille
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Informations sur le produit

5-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid methyl ester is a versatile compound recognized for its unique trifluoromethyl group, which enhances its chemical stability and lipophilicity. This compound is particularly valuable in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its distinctive structure allows for the development of novel compounds with improved biological activity, making it a crucial building block in drug discovery and development.

In addition to its applications in pharmaceuticals, this compound is also utilized in materials science, particularly in the formulation of advanced materials and coatings. Its ability to modify surface properties and enhance performance characteristics makes it an attractive option for researchers and industry professionals looking to innovate in their respective fields. The trifluoromethyl group not only contributes to the compound's unique properties but also offers advantages over similar compounds, such as increased potency and selectivity in biological applications.

Numéro CAS 
146137-92-0
Formule moléculaire
C11H7F3O2S
Poids moléculaire 
260.23
Informations générales
Numéro CAS 
146137-92-0
Formule moléculaire
C11H7F3O2S
Poids moléculaire 
260.23
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

5-(Trifluoromethyl)benzo[b]thiophene-2-carboxylic acid methyl ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting specific biological pathways due to its unique trifluoromethyl group, which enhances biological activity.
  • Material Science: It is used in the development of advanced materials, including polymers and coatings, where its properties can improve durability and resistance to environmental factors.
  • Agricultural Chemicals: The compound is explored in the formulation of agrochemicals, providing effective solutions for pest control while minimizing environmental impact.
  • Fluorinated Compounds Research: As a fluorinated compound, it is valuable in studies related to the effects of fluorine in organic chemistry, offering insights into reactivity and stability.
  • Analytical Chemistry: It is utilized as a reference standard in analytical methods, aiding in the accurate detection and quantification of similar compounds in complex mixtures.

Citations