CAS 56621-48-8

N-(4-Hidroxifenil)piperazina

Descrição:

N-(4-Hidroxifenil)piperazina, com o número CAS 56621-48-8, é um composto orgânico caracterizado por seu núcleo de piperazina, que é um anel de seis membros contendo dois átomos de nitrogênio. Este composto apresenta um grupo hidroxila (-OH) ligado a um anel fenil na posição para, contribuindo para suas propriedades químicas. Normalmente é um sólido branco a off-white e é solúvel em solventes polares como água e álcoois, devido à presença do grupo hidroxila. O composto exibe potencial atividade biológica, tornando-o de interesse na química medicinal, particularmente no desenvolvimento de produtos farmacêuticos. Sua estrutura permite interações com vários alvos biológicos, que podem incluir receptores de neurotransmissores. Além disso, N-(4-Hidroxifenil)piperazina pode participar de várias reações químicas, incluindo substituições e reações de acoplamento, tornando-o um intermediário versátil na síntese orgânica. Devem ser observadas precauções de segurança e manuseio, como com qualquer substância química, devido à potencial toxicidade ou reatividade.

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

Chave 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%

1-(4-Hydroxyphenyl)piperazine

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Pureza: >98.0%(GC)

Cor e Forma: Light yellow to Brown powder to crystal

Peso molecular: 178.24

Ref: 3B-H0891

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%

Cor e Forma: 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%

Cor e Forma: Solid

Peso molecular: 178.2310

Ref: IN-DA003CZW

1-(4-Hydroxyphenyl)piperazine

Produto Controlado

CAS: 56621-48-8

Applications 1-(4-Hydroxyphenyl)piperazine

Fórmula: C₁₀H₁₄N₂O

Cor e Forma: Neat

Peso molecular: 178.23

Ref: TR-H952888

4-(Piperazin-1-yl)phenol

CAS: 56621-48-8

Fórmula: C₁₀H₁₄N₂O

Pureza: 97%

Peso molecular: 178.23

Ref: IN-DG12212

4-(Piperazin-1-yl)phenol

CAS: 56621-48-8

4-(Piperazin-1-yl)phenol

Fórmula: C₁₀H₁₄N₂O

Pureza: >98%

Cor e Forma: Pale brown Solid-Powder

Peso molecular: 178.23096

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%

Cor e Forma: Solid

Peso molecular: 178.235

Ref: 10-F009797

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