cas 34117-90-3|| where to buy 3-chloroquinoxalin-2-amine

Nom du produit:3-chloroquinoxalin-2-amine

IUPAC Name:3-chloroquinoxalin-2-amine

: CAS：34117-90-3; Formule moléculaire：C8H6ClN3; Pureté：98%

: Numéro de catalogue：CM107805; Poids moléculaire：179.61

Unité d'emballage	Stock disponible	Prix($)
CM107805-1g	in stock	ǵŉȎ
CM107805-5g	in stock	ĽǊĽ

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Détails du produit

: N° CAS:34117-90-3; Formule moléculaire:C8H6ClN3; Point de fusion:-; Code SMILES:NC1=NC2=CC=CC=C2N=C1Cl; Densité:

: Numéro de catalogue:CM107805; Poids moléculaire:179.61; Point d'ébullition:289°C at 760 mmHg; N° Mdl:MFCD00234398; Stockage:Keep in dark place, store at 2-8°C.

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.

Column Infos

: Quinoxalines

Product Other Information

Product Overview	3-chloroquinoxalin-2-amine, also known as 3-CQA, is an organic compound with a wide range of applications in scientific research. It has been used in the synthesis of various compounds, as well as in the study of biochemical and physiological effects.
Synthesis and Application	3-chloroquinoxalin-2-amine can be synthesized in a variety of ways. One method involves the reaction of 2-chloroquinoxaline with ethyl chloroformate, followed by a hydrolysis. Another method involves the reaction of 2-chloroquinoxaline with ethyl chloroformate and sodium hydroxide, followed by a hydrolysis. Additionally, 3-chloroquinoxalin-2-amine can be synthesized from 2-chloroquinoxaline and ethyl chloroformate in the presence of a base such as pyridine or triethylamine. 3-chloroquinoxalin-2-amine has been used in a variety of scientific research applications. It has been used in the synthesis of various compounds, such as quinoxaline derivatives and hydrazines. Additionally, it has been used in the study of biochemical and physiological effects, such as the inhibition of enzyme activity and the modulation of ion channels. 3-chloroquinoxalin-2-amine has also been used in the study of the pharmacological effects of various compounds, and in the development of potential therapeutic agents.
Future Directions	Given the potential applications of 3-chloroquinoxalin-2-amine in scientific research, there are a number of potential future directions for its use. These include further studies of its mechanism of action, biochemical and physiological effects, and potential therapeutic applications. Additionally, 3-chloroquinoxalin-2-amine could be used in the development of new compounds and drugs, and in the study of the pharmacological effects of various compounds. Finally, 3-chloroquinoxalin-2-amine could be used in the development of new diagnostic tools and treatments for various diseases.