CAS 56621-48-8

N-(4-Hidroxifenil)piperazina

Descripción:

N-(4-Hidroxifenil)piperazina, con el número CAS 56621-48-8, es un compuesto orgánico caracterizado por su núcleo de piperazina, que es un anillo de seis miembros que contiene dos átomos de nitrógeno. Este compuesto presenta un grupo hidroxilo (-OH) unido a un anillo fenilo en la posición para, lo que contribuye a sus propiedades químicas. Típicamente es un sólido blanco a blanco sucio y es soluble en disolventes polares como agua y alcoholes, debido a la presencia del grupo hidroxilo. El compuesto exhibe una actividad biológica potencial, lo que lo hace de interés en la química medicinal, particularmente en el desarrollo de productos farmacéuticos. Su estructura permite interacciones con varios objetivos biológicos, que pueden incluir receptores de neurotransmisores. Además, N-(4-Hidroxifenil)piperazina puede participar en varias reacciones químicas, incluidas sustituciones y reacciones de acoplamiento, lo que lo convierte en un intermediario versátil en la síntesis orgánica. Se deben observar precauciones de seguridad y manejo, como con cualquier sustancia química, debido a la posible toxicidad o reactividad.

Fórmula: C₁₀H₁₄N₂O

InChI: InChI=1/C10H14N2O/c13-10-3-1-9(2-4-10)12-7-5-11-6-8-12/h1-4,11,13H,5-8H2

Clave InChI: InChIKey=GPEOAEVZTOQXLG-UHFFFAOYSA-N

SMILES: OC1=CC=C(C=C1)N2CCNCC2

Sinónimos:

• 1-(4-Hydroxyphenyl)piperazine
• 4-(1-Piperazino)phenol
• 4-(1-Piperazinyl)phenol
• 4-(4-Hydroxyphenyl)piperazine
• 4-(Piperazin-1-Yl)Phenol
• 4-Hydroxy Phenyl Piperazine
• 4-Piperazinophenol
• Phenol, 4-(1-piperazinyl)-
• N-(4-Hydroxyphenyl)piperazine
• RARECHEM AH CK 0119
• 1-(4-HYDROXYPHENYL)PIPERAZINE HYDROCHLORIDE
• p-(1-piperazinyl)phenol
• 1-(4-HYDROXYPHENYL)PROPERAZINE
• 1-(4-Hydroxyphenyl)piperazine 98%
• Phenol, 4-(1-piperazinyl)-(9CI)
• LABOTEST-BB LT00233198
• 4-(1-Piperazino)phenol,98%
• SALOR-INT L497754-1EA
• 4-(1-PIPERAZINO)PHENOL 98%

4-(1-Piperazinyl)phenol, 95%

CAS: 56621-48-8

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Fórmula: C₁₀H₁₄N₂O

Pureza: 95%

Forma y color: Powder, Pale brown to brown or pink

Peso molecular: 178.24

Ref: 02-B20122

4-(Piperazin-1-yl)phenol

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Pureza: 97%

Forma y color: Solid

Peso molecular: 178.2310

Ref: IN-DA003CZW

1-(4-Hydroxyphenyl)piperazine

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Pureza: >98.0%(GC)

Forma y color: Light yellow to Brown powder to crystal

Peso molecular: 178.24

Ref: 3B-H0891

4-(Piperazin-1-yl)phenol

CAS: 56621-48-8

4-(Piperazin-1-yl)phenol

Fórmula: C₁₀H₁₄N₂O

Pureza: 98%

Forma y color: beige solid

Peso molecular: 178.23g/mol

Ref: 54-OR6840

Posaconazole Impurity 128

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Peso molecular: 178.24

Ref: 4Z-P-38161

Posaconazole Impurity 96

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Peso molecular: 178.24

Ref: ST-EA-CP-P24074

1-(4-Hydroxyphenyl)-piperazine

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Pureza: 97%

Forma y color: Crystalline

Peso molecular: 178.235

Ref: 10-F009797

1-(4-Hydroxyphenyl)piperazine

Producto controlado

CAS: 56621-48-8

Applications 1-(4-Hydroxyphenyl)piperazine

Fórmula: C₁₀H₁₄N₂O

Forma y color: Neat

Peso molecular: 178.23

Ref: TR-H952888

1-(4-Hydroxyphenyl)piperazine

CAS: 56621-48-8

1-(4-Hydroxyphenyl)piperazine (HPP) is a drug that is metabolized by the liver cytochrome P450 system. It inhibits the oxidation of coumarin derivatives and facilitates their coupling with hydroxyl groups, which results in the formation of 1-hydroxy-2-oxo-3-(4-hydroxyphenyl)piperazines. HPP has been shown to inhibit hepatic cytochrome P450 in humans, as well as mouse liver microsomes. This inhibition can be reversed by adding chemical inhibitors such as phenobarbital or aminopyrine. HPP also catalyzes glutaminyl cyclase to form glutaminyl amino acids, and is involved in the production of heme, which may be due to its ferroelectric properties. HPP has been shown to be effective against spermatogenesis in male rats, and it was found that HPP was excreted from human

Fórmula: C₁₀H₁₄N₂O

Pureza: Min. 95%

Peso molecular: 178.23 g/mol

Ref: 3D-FH75439