cas 928664-14-6|| where to buy 4-Fluoroisoquinolin-5-amine

Produktname:4-Fluoroisoquinolin-5-amine

IUPAC Name:4-fluoroisoquinolin-5-amine

: CAS：928664-14-6; Molekulare Formel：C9H7FN2; Reinheit：95%

: Katalognummer：CM223002; Molekulargewicht：162.17

Packungseinheit	Verfügbarer Vorrat	Preis($)
CM223002-100mg	in stock	ŌƚŤ
CM223002-250mg	in stock	ŤǸǪ
CM223002-1g	in stock	ǸŌǸǪ

Anfrage: sales@chemenu.com

Nur für den Einsatz in Forschung und Entwicklung..

Anfrage-Formular

Chemische Bezeichnung

CAS-Nummer

Menge*

Erforderliche Spezifikationen*
(Gehalt %, Materialqualität etc.)

Name des Ansprechpartners*

E-Mail des Ansprechpartners*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 928664-14-6 regularly via the above email.

Zusätzliche Hinweise

Verification code*

refresh

Produkt-Details

: CAS-Nr.:928664-14-6; Molekulare Formel:C9H7FN2; Schmelzpunkt:-; SMILES-Code:NC1=CC=CC2=C1C(F)=CN=C2; Dichte:

: Katalognummer:CM223002; Molekulargewicht:162.17; Siedepunkt:; Mdl-Nr.:MFCD20696998; Lagerung:

Category Infos

: Isoquinolines; Compared to quinolines, isoquinolines are also prominent structural motifs present in many biologically significant natural and synthetic compounds. Some well-known isoquinoline alkaloids include the anticancer and anticonvulsant berberine, the vasodilator and antispasmodic drugs papaverine and emetine. In addition to naturally occurring isoquinolines, synthetic analogs have also shown significant biological activity.

Product Other Information

Product Overview	4-Fluoroisoquinolin-5-amine is an organic compound that has gained attention in the scientific community due to its potential applications in drug discovery and development. This compound has been found to exhibit a wide range of biological activities, including anti-tumor, anti-inflammatory, and anti-viral properties.
Synthesis and Application	The synthesis of 4-Fluoroisoquinolin-5-amine involves a multi-step process that has been described in several research articles. The most common method involves the reaction of 4-Fluoroaniline with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) in the presence of a base such as potassium carbonate. The resulting product is then treated with hydrochloric acid to yield 4-Fluoroisoquinolin-5-amine. 4-Fluoroisoquinolin-5-amine has been extensively studied for its potential applications in drug discovery and development. Several research studies have reported its anti-tumor properties against various cancer cell lines, including breast cancer, lung cancer, and leukemia. It has also been found to exhibit anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines. Additionally, 4-Fluoroisoquinolin-5-amine has been shown to have anti-viral activity against the hepatitis C virus.
Future Directions	There are several future directions for research on 4-Fluoroisoquinolin-5-amine. One area of interest is the development of new derivatives of this compound with improved pharmacological properties. Another area of research is the investigation of the mechanism of action of 4-Fluoroisoquinolin-5-amine, which can provide insights into its biological activities. Additionally, the potential use of 4-Fluoroisoquinolin-5-amine in the treatment of viral infections such as hepatitis C is an area of ongoing research.