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1-Acetylpiperazine

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1-Acetylpiperazine Basic information

Product Name:
1-Acetylpiperazine
Synonyms:
  • N-ACETYLPIPERAZINE
  • AKOS BB-5737
  • 1-ACETYLPIPERAZINE
  • 1-PIPERAZIN-1-YL-ETHANONE
  • 1-AcetyL
  • acetylpiperazine
  • N-Acetylpiperazine97%
  • N-Acetylpiperazine,99%
CAS:
13889-98-0
MF:
C6H12N2O
MW:
128.17
EINECS:
237-659-0
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Piperidines, Piperidones, Piperazines
  • Piperaizine
  • API intermediates
  • Piperazines
Mol File:
13889-98-0.mol
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1-Acetylpiperazine Chemical Properties

Melting point:
31-34 °C (lit.)
Boiling point:
127 °C
Density 
1.0754 (rough estimate)
refractive index 
1.4880 (estimate)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
methanol: soluble1g/10 mL, clear, colorless to faintly greenish-yellow
pka
8.50±0.10(Predicted)
form 
Liquid After Melting
color 
Clear light yellow
Water Solubility 
Soluble in water 210 g/L (20°C).
Sensitive 
Hygroscopic
BRN 
112220
CAS DataBase Reference
13889-98-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/38-36/37/38
Safety Statements 
26-36-37/39
WGK Germany 
3
3-10-34
Hazard Note 
Irritant
HS Code 
29339900

MSDS

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1-Acetylpiperazine Usage And Synthesis

Chemical Properties

clear light yellow liquid after melting

Uses

1-Acetylpiperazine may be used in the synthesis of series of 7-alkoxyl substituted indolizinoquinoline-5,12-dione derivatives and 2-substituted-N-(naphth-1-ylmethyl)-pyrimidin-4-amines and 2-substituted-N-benzhydrylpyrimidin-4-amines.

Definition

ChEBI: 1-Acetylpiperazine is a member of phytanoyl-CoAs.

General Description

Infrared and Raman spectra of 1-acetylpiperazine have been recorded in the region of 4000-40cm-1.

Purification Methods

Purify 1-acetylpiperazine by recrystallisation from 40% aqueous EtOH or from EtOH/Et2O. It is an irritant, and is hygroscopic. The hydrochloride has m 191o (from EtOH), and the tosylate salt has m 148-149o (from EtOH/EtOAc, 1:16). The free base, however, cannot be isolated by basifying the tosylate salt and extraction with CH2Cl2. [Jacobi Chem Ber 66 113 1933, Mosher et al. J Am Chem Soc 75 4949 1953, Hall J Am Chem Soc 78 2570 1956, Beilstein 23 IV 1786.]

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