cas 6956-30-5|| where to buy 2-Chloro-3-((2-(piperazin-1-yl)ethyl)amino)naphthalene-1,4-dione

Produktname:2-Chloro-3-((2-(piperazin-1-yl)ethyl)amino)naphthalene-1,4-dione

IUPAC Name:2-chloro-3-{[2-(piperazin-1-yl)ethyl]amino}-1,4-dihydronaphthalene-1,4-dione

Packungseinheit	Verfügbarer Vorrat	Preis($)	Menge

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 6956-30-5 regularly via the above email.

Zusätzliche Hinweise

Verification code*

refresh

: CAS-Nr.:6956-30-5; Molekulare Formel:C16H18ClN3O2; Schmelzpunkt:-; SMILES-Code:O=C1C(Cl)=C(NCCN2CCNCC2)C(C3=C1C=CC=C3)=O; Dichte:

: Katalognummer:CM264366; Molekulargewicht:319.79; Siedepunkt:; Mdl-Nr.:; Lagerung:

: Piperazines; Piperazine is an organic compound consisting of a six-membered ring containing two nitrogen atoms in opposite positions in the ring. The chemical formula of piperazine is C4H10N2, and it is an important pharmaceutical intermediate. Pyrimidines and piperazines are known to be the backbone of many bulk compounds and important core structures for approved drugs; studies have shown that combining a pyridine ring with a piperazine moiety within a single structural framework enhances biological activity.

: Quinones; The quinones are a class of organic compounds that are formally derived from aromatic compounds by conversion of an even number of –CH= groups into –C(=O)– groups with any necessary rearrangement of double bonds, resulting in a fully conjugated cyclic dione structure. Quinones exhibit numerous biological activities such as neurological, antibacterial, antiplasmodial, antioxidantal, trypanocidal, antitumor, and anti-HIV, and these activities have been proven to be related to the redox properties of their carbonyl functions.