Nombre del producto:1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine

IUPAC Name:1-[2-nitro-4-(trifluoromethyl)phenyl]piperidine

CAS:1692-79-1
Fórmula molecular:C12H13F3N2O2
Pureza:95%
Número de catálogo:CM180136
Peso molecular:274.24

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CM180136-500g 3-4 Weeks ǵNJƥ

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Detalles del producto

Núm. De CAS :1692-79-1
Fórmula molecular:C12H13F3N2O2
Punto de fusión:-
Código de sonrisas:[O-][N+](=O)C1=C(C=CC(=C1)C(F)(F)F)N1CCCCC1
Densidad:
Número de catálogo:CM180136
Peso molecular:274.24
Punto de ebullición:342.8°C at 760 mmHg
Nº Mdl:MFCD00052908
Almacenamiento:Store at 2-8°C.

Category Infos

Piperidines
Piperidine is an azacycloalkane that is cyclohexane in which one of the carbons is replaced by a nitrogen. Although piperidine is a common organic compound, it is an immensely important class of compounds medicinally: the piperidine ring is the most common heterocyclic subunit among FDA approved drugs.
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Product Overview 1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine, also known as 1-NTP, is an organic compound that is used in various scientific research applications. It is a nitrogen-containing heterocyclic compound that is derived from the piperidine family of compounds. 1-NTP has a wide range of uses in the laboratory, including synthesis, drug development, and biochemical research. This article will discuss the synthesis method, scientific research applications, mechanism of action, biochemical and physiological effects, advantages and limitations for lab experiments, and future directions of 1-NTP.
Synthesis and Application 1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine is synthesized through a multi-step process. The starting material for the synthesis is piperidine, which is reacted with nitroacetone in the presence of an acid catalyst to form 2-nitropiperidine. This intermediate is then reacted with trifluoromethyl iodide in the presence of a base catalyst to yield 1-[2-nitro-4-(trifluoromethyl)phenyl]piperidine. This reaction is carried out in an inert atmosphere to prevent the product from being degraded by oxygen. 1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine is used in a variety of scientific research applications, including drug development, biochemical research, and synthesis. It has been used as a substrate for the synthesis of various pharmaceuticals, such as the anti-cancer drug gefitinib. It has also been used in the synthesis of other heterocyclic compounds, such as pyridines, quinolines, and indoles. Additionally, 1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine has been used in biochemical research to study the structure and function of enzymes.
Future Directions The use of 1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine in scientific research is an area that is still being explored. Further research into its biochemical and physiological effects could lead to new applications for this compound. Additionally, further research into its synthesis and stability could lead to improvements in its use in laboratory experiments. Additionally, further research into its potential toxicity could help to identify potential safety concerns. Finally, further research into the metabolism of 1-[2-Nitro-4-(trifluoromethyl)phenyl]piperidine could lead to new insights into drug metabolism.