cas 2227206-64-4|| where to buy 6-amino-3λ⁶-thiabicyclo[3.1.0]hexane-3,3-dione hydrochloride

Produktname:6-amino-3λ⁶-thiabicyclo[3.1.0]hexane-3,3-dione hydrochloride

IUPAC Name:6-amino-3λ⁶-thiabicyclo[3.1.0]hexane-3,3-dione hydrochloride

: CAS：2227206-64-4; Molekulare Formel：C5H10ClNO2S; Reinheit：95%+

Packungseinheit	Verfügbarer Vorrat	Preis($)
CM1017748-100mg	in stock	Ȍǧƻ
CM1017748-250mg	in stock	ǧƻȷɅ
CM1017748-500mg	in stock	ǧƋƙƋ
CM1017748-1g	in stock	ƙƙƋƱ

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 2227206-64-4 regularly via the above email.

Zusätzliche Hinweise

Verification code*

refresh

: CAS-Nr.:2227206-64-4; Molekulare Formel:C5H10ClNO2S; Schmelzpunkt:-; SMILES-Code:Cl.NC1C2CS(=O)(=O)CC12; Dichte:

: Katalognummer:CM1017748; Molekulargewicht:183.65; Siedepunkt:; Mdl-Nr.:; Lagerung:

: Cyclopropanes; Cyclopropane is the smallest cyclic compound with unique structural features and physicochemical properties, which is widely used in the design of small molecule drugs. In drug design, it is often used to increase activity, fix conformation and improve PK and water solubility. The introduction of cyclopropyl groups into drugs can change various properties of molecules, such as improving metabolic stability; increasing biological activity; enhancing drug efficacy; limiting polypeptide conformation and slowing down its hydrolysis; reducing plasma clearance; improving drug dissociation and many more. Cyclopropane rings are widely found in marketed drugs, including cardiovascular drugs, central nervous system (CNS) drugs, anticancer drugs, autoimmune and anti-inflammatory drugs.

: Tetrahydrothiophenes; Tetrahydrothiophene is a sulfur-containing saturated heterocyclic compound obtained by catalytic hydrogenation of thiophene. After thiophene is reduced to tetrahydrothiophene, it no longer has a conjugated system and aromaticity. Therefore, tetrahydrothiophene shows the properties of general thioethers. Easily oxidized to sulfoxides and sulfones. Tetrahydrothiophene can be used as a raw material for the production of pharmaceuticals, pesticides and photochemicals.