ChemicalBook--->CAS DataBase List--->33422-35-4

33422-35-4

33422-35-4 Structure

33422-35-4 Structure
IdentificationMore
[Name]

ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE
[CAS]

33422-35-4
[Synonyms]

(3-OXO-PIPERAZIN-2-YL)-ACETIC ACID ETHYL ESTER
AKOS BBB/039
AKOS BC-0605
BUTTPARK 32\06-70
ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE
ETHYL 2-(3-OXOPIPERAZIN-2-YL)ACETATE
ETHYL (3-OXOPIPERAZIN-2-YL)ACETATE
TIMTEC-BB SBB010112
ETHYL 3-OXOPIPERAZINE-2-ACETATE
3-Oxo-2-piperazineacetic acid ethyl ester
[Molecular Formula]

C8H14N2O3
[MDL Number]

MFCD00052897
[Molecular Weight]

186.21
[MOL File]

33422-35-4.mol
Chemical PropertiesBack Directory
[Melting point ]

110-111°C
[Boiling point ]

360.6±27.0 °C(Predicted)
[density ]

1.101±0.06 g/cm3(Predicted)
[storage temp. ]

Keep in dark place,Sealed in dry,2-8°C
[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)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[Hazard Note ]

Irritant
[HazardClass ]

IRRITANT
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

ETHYL 2-(3-OXO-2-PIPERAZINYL)ACETATE(33422-35-4)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

ethyl 2-(3-oxo-2-piperazinyl)acetate(33422-35-4)
Hazard InformationBack Directory
[Synthesis]

Ethylenediamine

107-15-3

Diethyl maleate

141-05-9

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

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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