Basic information Safety Supplier Related

4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER

Basic information Safety Supplier Related

4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Basic information

Product Name:
4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
Synonyms:
  • 1-BOC-4-(2-AMINOETHYL)PIPERAZINE
  • 4-N-(2-AMINOETHYL)-1-N-BOC-PIPERAZINE
  • 4-(2-AMINO-ETHYL)-1-BOC-PIPERAZINE
  • 4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 4-(2-AMINOETHYL)PIPERAZINE, N1-BOC PROTECTED
  • TERT-BUTYL 4-(2-AMINOETHYL)PIPERAZINE-1-CARBOXYLATE
  • TERT-BUTYL 4-(2-AMINOETHYL)TETRAHYDRO-1(2H)-PYRAZINECARBOXYLATE
  • BUTTPARK 90\06-05
CAS:
192130-34-0
MF:
C11H23N3O2
MW:
229.32
Product Categories:
  • piperazines
  • pharmacetical
Mol File:
192130-34-0.mol
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4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Chemical Properties

Melting point:
36-41°C
Boiling point:
319.4±32.0 °C(Predicted)
Density 
1.056±0.06 g/cm3(Predicted)
Flash point:
>198℃
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
pka
10.11±0.10(Predicted)
form 
low melting solid
color 
Light yellow to yellow
InChI
InChI=1S/C11H23N3O2/c1-11(2,3)16-10(15)14-8-6-13(5-4-12)7-9-14/h4-9,12H2,1-3H3
InChIKey
QSYTWBKZNNEKPN-UHFFFAOYSA-N
SMILES
N1(C(OC(C)(C)C)=O)CCN(CCN)CC1
CAS DataBase Reference
192130-34-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
2933599590
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4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTER Usage And Synthesis

Uses

tert-Butyl 4-(2-aminoethyl)piperazine-1-carboxylate is a useful research chemical for the synthesis of biologically active compounds.

Synthesis

227776-28-5

192130-34-0

GENERAL METHOD: N-substituted phthalimide (2.00 mmol) was mixed with 80% aqueous hydrazine hydrate (2 mL) in ethanol (20 mL) and the reaction was stirred at 70°C for 20 hours. After completion of the reaction, the mixture was cooled to room temperature and filtered to remove the precipitate. The filtrate was concentrated under reduced pressure to remove the solvent to give the crude product, which can be used directly in subsequent reactions without further purification.

References

[1] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 7, p. 2251 - 2259
[2] ChemMedChem, 2014, vol. 9, # 4, p. 752 - 761

4-(2-AMINO-ETHYL)-PIPERAZINE-1-CARBOXYLIC ACID TERT-BUTYL ESTERSupplier

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