Nombre del producto:1,2,3,4-Tetrahydro-quinoxaline-6-carboxylic acid

IUPAC Name:1,2,3,4-tetrahydroquinoxaline-6-carboxylic acid

CAS:787490-63-5
Fórmula molecular:C9H10N2O2
Pureza:95%
Número de catálogo:CM141850
Peso molecular:178.19

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Detalles del producto

Núm. De CAS :787490-63-5
Fórmula molecular:C9H10N2O2
Punto de fusión:-
Código de sonrisas:O=C(C1=CC2=C(NCCN2)C=C1)O
Densidad:
Número de catálogo:CM141850
Peso molecular:178.19
Punto de ebullición:
Nº Mdl:MFCD09832508
Almacenamiento:

Category Infos

Quinoxalines
Quinoxalines, also known as benzopyrazines, are heterocyclic compounds containing a ring complex consisting of a benzene ring and a pyrazine ring. It has isomerism with other naphthalene compounds such as quinazoline, phthalazine, cinnamine, etc. Fusion N-heterocyclic compounds are widely used as valuable entities for the expansion of important pharmacological agents and are considered to be an advantageous scaffold material. Among the numerous fused N-heterocyclic compounds, cinnoline, quinoxaline and quinazoline are important pharmacological agents. In medicinal chemistry, these N-heterocyclic compounds have a wide range of biological properties and can be used as synthetic intermediates, potential drug candidates and chemical probes.
Benzenes
Benzene is an important organic compound with the chemical formula C6H6, and its molecule consists of a ring of 6 carbon atoms, each with 1 hydrogen atom. Benzene is a sweet, flammable, colorless and transparent liquid with carcinogenic toxicity at room temperature, and has a strong aromatic odor. It is insoluble in water, easily soluble in organic solvents, and can also be used as an organic solvent itself. The ring system of benzene is called benzene ring, and the structure after removing one hydrogen atom from the benzene ring is called phenyl. Benzene is one of the most important basic organic chemical raw materials. Many important chemical intermediates can be derived from benzene through substitution reaction, addition reaction and benzene ring cleavage reaction.

Column Infos