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Catalog Number:
45007
CAS Number:
104366-23-6
2-Amino-4-cloro-5-formil-3-tiofenocarbonitrilo
Purity:
≥ 98% (GC)
Synonym(s):
2-Amino-4-cloro-3-ciano-5-formiltiofeno
Hazmat
Documents
$104.96 /1G
Tamaño
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Información del producto

2-Amino-4-chloro-5-formyl-3-thiophenecarbonitrile is a versatile compound with significant potential in various fields, particularly in organic synthesis and pharmaceuticals. This compound features a unique thiophene ring structure, which enhances its reactivity and makes it an excellent candidate for developing novel materials and bioactive molecules. Its amino and formyl functional groups contribute to its utility in the synthesis of complex organic compounds, allowing researchers to explore new pathways in drug discovery and development.

In the pharmaceutical industry, 2-Amino-4-chloro-5-formyl-3-thiophenecarbonitrile can be utilized in the design of targeted therapies due to its ability to interact with biological systems. Its chlorinated structure may also impart unique properties that can be advantageous in creating compounds with improved efficacy and reduced side effects. Researchers and industry professionals can leverage this compound for applications in medicinal chemistry, agrochemicals, and material science, making it a valuable addition to any laboratory focused on innovative chemical solutions.

Número CAS
104366-23-6
Fórmula molecular
C6H3ClN2SO
Peso molecular
0
Número MDL
MFCD03788265
Punto de fusión
269 °C (descenso)
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
104366-23-6
Fórmula molecular
C6H3ClN2SO
Peso molecular
0
Número MDL
MFCD03788265
Punto de fusión
269 °C (descenso)
Condiciones
Conservar entre 2 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

2-Amino-4-chloro-5-formyl-3-thiophenecarbonitrile is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly those targeting anti-inflammatory and anti-cancer activities.
  • Organic Synthesis: It is frequently employed in organic chemistry for the preparation of thiophene derivatives, which are valuable in the development of new materials and compounds.
  • Biological Research: Researchers use this chemical to study its biological properties, contributing to the understanding of its potential therapeutic effects and mechanisms of action.
  • Material Science: The compound is explored for its applications in creating conductive polymers and other advanced materials, enhancing the performance of electronic devices.
  • Analytical Chemistry: It is utilized as a reagent in various analytical techniques, aiding in the detection and quantification of other chemical species in complex mixtures.

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