cas 1222974-62-0|| where to buy 2-{1-methyl-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazin-2-yl}-N-(2,2,2-trifluoroethyl)acetamide

Nombre del producto:2-{1-methyl-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazin-2-yl}-N-(2,2,2-trifluoroethyl)acetamide

IUPAC Name:2-{1-methyl-1H,2H,3H,4H-pyrrolo[1,2-a]pyrazin-2-yl}-N-(2,2,2-trifluoroethyl)acetamide

: CAS：1222974-62-0; Fórmula molecular：C12H16F3N3O; Pureza：95%+

: Número de catálogo：CM1024493; Peso molecular：275.27

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Detalles del producto

: Núm. De CAS :1222974-62-0; Fórmula molecular:C12H16F3N3O; Punto de fusión:-; Código de sonrisas:CC1N(CC(=O)NCC(F)(F)F)CCN2C=CC=C12; Densidad:

: Número de catálogo:CM1024493; Peso molecular:275.27; Punto de ebullición:; Nº Mdl:; Almacenamiento:

Category Infos

: Fluorinated Compounds; Fluorine is the most electronegative element in the periodic table, and the fluorine atom has a small atomic radius, so fluorine-containing organic compounds have many wonderful properties. For example, the introduction of fluorine atoms or fluorine-containing groups into drug molecules can improve the permeability to cell membranes, metabolic stability and bioavailability; in addition, the introduction of fluorine atoms will improve the lipid solubility of the compound and promote its absorption in the body. The speed of delivery changes the physiological effect. In the field of medicinal chemistry, the introduction of fluorine atoms into organic molecules is an important direction for the development of new anticancer drugs, antitumor drugs, antiviral agents, anti-inflammatory drugs, and central nervous system drugs.

: Pyrrolopyrazines; Nitrogen-containing heterocyclic compounds have a wide range of applications in medicine, organic materials, natural products and other fields, mainly for biologically active molecules. Pyrrolopyrazines contain pyrrole and pyrazine rings as bioactive scaffolds. Compounds containing this scaffold have a wide range of biological activities, such as antibacterial, anti-inflammatory, antiviral, antifungal, antioxidant, antitumor, and kinase inhibition.

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