Home Categories Pharmaceutical intermediates Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate
BD9278531

Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate , 97% , 184177-81-9

CAS NO.:184177-81-9

Empirical Formula: C23H23N3O3

Molecular Weight: 389.45

MDL number: MFCD03784249

Pack Size Price Stock Quantity
1g RMB24.00 In Stock
5g RMB28.80 In Stock
25g RMB118.40 In Stock
100g RMB428.80 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Boiling point: 603.9±55.0 °C(Predicted)
Density  1.296
storage temp.  Sealed in dry,Room Temperature
pka 12.18±0.30(Predicted)
InChI InChI=1S/C23H23N3O3/c27-21-12-10-20(11-13-21)26-16-14-25(15-17-26)19-8-6-18(7-9-19)24-23(28)29-22-4-2-1-3-5-22/h1-13,27H,14-17H2,(H,24,28)
InChIKey IKRKMYDCUZYKHX-UHFFFAOYSA-N
SMILES C(OC1=CC=CC=C1)(=O)NC1=CC=C(N2CCN(C3=CC=C(O)C=C3)CC2)C=C1

Description and Uses

Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate is a piperazine derivative that inhibits the growth of gram-positive bacteria.Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)phenyl)carbamate is a carbamic acid that binds to the 50S ribosomal subunit of bacteria, preventing transcription and replication. Phenyl (4-(4-(4-hydroxyphenyl)piperazin-1-yl)) carbamate is a carbamic acid that binds to the 50S ribosomal subunit of bacteria, preventing transcription and replication. Human activity on human erythrocytes using the membrane clamp technique is frequent. This active form is metabolised by a number of metabolic transformations including hydrolysis by esterases or glucuronidases, oxidation by cytochrome P450 enzymes, reduction by glutathione reductase, or binding to glucuronic acid.

[4-[4-(4-Hydroxyphenyl)-1-piperazinyl]phenyl]carbamic Acid Phenyl Ester is an impurity of Posaconazole (P689600), which is orally active antifungal triazole.

Safety

Symbol(GHS) 
GHS09
Signal word  Warning
Hazard statements  H410
Precautionary statements  P273-P391-P501

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