Basic information Safety Supplier Related

ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE

Basic information Safety Supplier Related

ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE Basic information

Product Name:
ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE
Synonyms:
  • TIMTEC-BB SBB010112
  • ETHYL 3-OXOPIPERAZINE-2-ACETATE
  • ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE
  • ETHYL 2-(3-OXOPIPERAZIN-2-YL)ACETATE
  • ETHYL (3-OXOPIPERAZIN-2-YL)ACETATE
  • BUTTPARK 32\06-70
  • (3-OXO-PIPERAZIN-2-YL)-ACETIC ACID ETHYL ESTER
  • AKOS BC-0605
CAS:
33422-35-4
MF:
C8H14N2O3
MW:
186.21
Product Categories:
  • pharmacetical
  • Esters
  • Pyrans, Piperidines &Piperazines
  • CHIRAL CHEMICALS
  • Pyrans, Piperidines & Piperazines
Mol File:
33422-35-4.mol
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ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE Chemical Properties

Melting point:
110-111°C
Boiling point:
360.6±27.0 °C(Predicted)
Density 
1.101±0.06 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
pka
15.06±0.40(Predicted)
Appearance
White to off-white Solid
InChI
InChI=1S/C8H14N2O3/c1-2-13-7(11)5-6-8(12)10-4-3-9-6/h6,9H,2-5H2,1H3,(H,10,12)
InChIKey
HNYRNJAZRKCHSC-UHFFFAOYSA-N
SMILES
N1CCNC(=O)C1CC(OCC)=O
CAS DataBase Reference
33422-35-4(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
HazardClass 
IRRITANT
HS Code 
2933599590
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ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE Usage And Synthesis

Synthesis

107-15-3

141-05-9

33422-35-4

1. Ethylenediamine (1.17 mL, 17.42 mmol) and diethyl maleate (3 g, 17.42 mmol) were added to a 50 mL round bottom flask and dissolved in propanol (30 mL). 2. The reaction mixture was stirred at 55 °C for 16 h. 3. Upon completion of the reaction, the solvent was removed under reduced pressure by rotary evaporator. 4. The residue was placed in a vacuum drying chamber and The residue was dried to give the crude ethyl 2-(3-oxopiperazin-2-yl)acetate. 5. The crude product was used directly in the next step of the reaction without further purification. Yield: 3.4 g (quantitative yield).

References

[1] Patent: US2008/312231, 2008, A1. Location in patent: Page/Page column 40
[2] Journal of Heterocyclic Chemistry, 1993, vol. 30, # 1, p. 275 - 276
[3] Journal of Pharmaceutical Sciences, 1990, vol. 79, # 5, p. 447 - 452

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