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Home > Encyclopedia > 1-Acetyl-4-(4-hydroxyphenyl)piperazine

1-Acetyl-4-(4-hydroxyphenyl)piperazine

1-Acetyl-4-(4-hydroxyphenyl)piperazine structure

1-Acetyl-4-(4-hydroxyphenyl)piperazine 

structure
  • CAS No:

    67914-60-7

  • Formula:

    C12H16N2O2

  • Chemical Name:

    1-Acetyl-4-(4-hydroxyphenyl)piperazine

  • Synonyms:

    Ethanone,1-[4-(4-hydroxyphenyl)-1-piperazinyl]-;Piperazine,1-acetyl-4-(4-hydroxyphenyl)-;1-[4-(4-Hydroxyphenyl)-1-piperazinyl]ethanone;T 1141;1-Acetyl-4-(p-hydroxyphenyl)piperazine;1-Acetyl-4-(4-hydroxyphenyl)piperazine;4-(4-Acetylpiperazino)phenol;1-[4-(4-Hydroxyphenyl)piperazin-1-yl]ethanone;4-(4-Acetylpiperazin-1-yl)phenol;1-[4-(4-Hydroxyphenyl)piperazin-1-yl]ethan-1-one;1229612-23-0

  • Categories:

    Chemical Reagents  >  Organic Reagents

Description

Off-White Solid

1-Acetyl-4-(4-hydroxyphenyl)piperazine Basic Attributes

220.27

220.27

795777

267-744-8

DTXSID3057804

29214910

Characteristics

43.8

0.19

White to slightly pink or beige Powder

1.2±0.1 g/cm3

180 °C @ Solvent: Ethanol

456.5±40.0 °C at 760 mmHg

229.9±27.3 °C

1.585

H2O: 4.3 g/L (20 ºC)

-20°C Freezer

Safety Information

NONH for all modes of transport

3

36/37/38-22

26-36-36/37/39-22

Xi,Xn

Stable under normal temperatures and pressures.

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (96%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 50 companies from 8 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

1-(4-(4-hydroxyphenyl)piperazin-1-yl)ethanone

1-Acetyl-4-(4-hydroxyphenyl)piperazine Use and Manufacturing

Methods of Manufacturing

Piperazine hexahydrate can be first condensed with p-nitrochlorobenzene to generate 1-(4-nitrophenyl)piperazine, and then react with acetic anhydride to obtain 1-acetyl-4-(4-nitrophenyl)piper Oxazine, the latter is obtained after nitro reduction, diazotization, and hydrolysis.

Uses

Used in the synthesis of ketoconazole and itraconazole

Computed Properties

Molecular Weight:220.27
XLogP3:1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:220.121177757
Monoisotopic Mass:220.121177757
Topological Polar Surface Area:43.8
Heavy Atom Count:16
Complexity:241
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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