Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate CAS 184177-81-9 Posaconazole Intermediate High Quality

Description:

Chemical Name: Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl) phenyl) carbamate

CAS: 184177-81-9

Intermedia Posaconazole (CAS 171228-49-2) Triazole Antifungal Agent

High Quality, Commercial Production

Inquiry: alvin@ruifuchem.com


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Descriptio:

Chemical Properties:

Nomen chemicum Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl) phenyl) carbamate
Synonyma Posaconazole medium
CAS Number 184177-81-9
CATTUS Number RF-PI290
Stock Status In Stock, Productio Ascendite ad Tons
Formulae hypotheticae C23H23N3O3
M. Pondus 389.45
Density 1.296
Shipping Condition Sub Ambient Temperature
Brand Ruifu Chemical

Specifications:

Item Specifications
Aspectus Palea Brown ad Grey pulveris
Puritas / Analysis Methodus ≥99.0% (HPLC)
Damnum in Siccatio ≤0.50%
Residere in Ignition ≤0.20%
Metalla gravis ≤20ppm
una immunditia ≤0.50%
Totalis immunditias ≤1.0%
Test Standard Enterprise Standard
Consuetudinem Posaconazole (CAS 171228-49-2).

Sarcina & Repono:

sarcina: Utrem, aluminium foil, pera, cardboard tympanum, 25kg/Drum, vel secundum exigentiam emptoris.

Repono Condition:Repone in vasis signatis in loco frigido et sicco;Protege a lumine, umore et peste infestatione.

commoda:

1

FAQ:

Applicatio:

Phenyl (4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamatum (CAS 184177-81-9) est medium Posaconazole (CAS 171228-49-2).Posaconazole est latum-spectrum, generatio secunda, triazolum compositum cum actione antifungali.Probata medicinae usu in Civitatibus Foederatis Americae Septembri MMVI, et medicamentum genericum praesto est.Posaconazole est triazolum antifungal pharmacum in Civitatibus Foederatis mercatum in Civitatibus Foederatis a Schering-Aro sub commercii nomine Noxafil.Posaconazolus operatur arctam sarcinam acyl catenarum phospholipidorum perturbando, functiones aliquas systematis enzyme ligatorum membranaceo incorrupto, sicut ATPase et enzymes electronici systematis onerarii, sic fungos incrementum inhibens.Hoc facit, impediendo synthesim ergosteroli, inhibendo enzyme lanosteroli 14a-demethylase et accumulationis praecursores methylati steroli.

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