cas 1351614-95-3|| where to buy N-[2-(4-{2-[4-(propan-2-ylsulfanyl)phenyl]acetyl}piperazin-1-yl)ethyl]thiophene-2-carboxamide hydrochloride

Nombre del producto:N-[2-(4-{2-[4-(propan-2-ylsulfanyl)phenyl]acetyl}piperazin-1-yl)ethyl]thiophene-2-carboxamide hydrochloride

IUPAC Name:N-[2-(4-{2-[4-(propan-2-ylsulfanyl)phenyl]acetyl}piperazin-1-yl)ethyl]thiophene-2-carboxamide hydrochloride

: CAS：1351614-95-3; Fórmula molecular：C22H30ClN3O2S2; Pureza：95%+

Unidad de embalaje	Stock disponible	Precio($)	Cantidad

Sólo para uso en I+D..

Formulario de consulta

Nombre químico

Número CAS

Cantidad*

Especificaciones requeridas*
(% de ensayo, grado de material, etc.)

Nombre de contacto*

Correo electrónico de contacto*

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 1351614-95-3 regularly via the above email.

Notas adicionales

Verification code*

refresh

: Núm. De CAS :1351614-95-3; Fórmula molecular:C22H30ClN3O2S2; Punto de fusión:-; Código de sonrisas:Cl.CC(C)SC1=CC=C(CC(=O)N2CCN(CCNC(=O)C3=CC=CS3)CC2)C=C1; Densidad:

: Número de catálogo:CM974196; Peso molecular:468.07; Punto de ebullición:; Nº Mdl:; Almacenamiento:

: Thiophenes; Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.

: 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.