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1-ISOPROPYL-PIPERIDIN-4-YLAMINE

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1-ISOPROPYL-PIPERIDIN-4-YLAMINE Basic information

Product Name:
1-ISOPROPYL-PIPERIDIN-4-YLAMINE
Synonyms:
  • 4-Piperidinamine, 1-(1-methylethyl)-
  • 1-isopropylpiperidin-4-amine(SALTDATA: 1.98HCl 0.34H2O)
  • 1-isopropylpiperidin-4-amine 1.98HCl 0.34H2O
  • 1-(propan-2-yl)piperidin-4-aMine
  • (1-isopropyl-4-piperidyl)amine
  • 1-(Prop-2-yl)piperidin-4-amine, 1-Isopropylpiperidin-4-amine
  • 1-Isopropyl-4-PiperidinaMine
  • 1-ISOPROPYLPIPERIDIN-4-AMINE
CAS:
127285-08-9
MF:
C8H18N2
MW:
142.24
Product Categories:
  • Heterocycles
Mol File:
127285-08-9.mol
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1-ISOPROPYL-PIPERIDIN-4-YLAMINE Chemical Properties

Boiling point:
173.2±8.0 °C(Predicted)
Density 
0.904±0.06 g/cm3(Predicted)
refractive index 
1.4720 to 1.4760
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
form 
clear liquid
pka
10.51±0.20(Predicted)
color 
Colorless to Almost colorless
InChI
InChI=1S/C8H18N2/c1-7(2)10-5-3-8(9)4-6-10/h7-8H,3-6,9H2,1-2H3
InChIKey
ZRQQXFMGYSOKDF-UHFFFAOYSA-N
SMILES
N1(C(C)C)CCC(N)CC1
CAS DataBase Reference
127285-08-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi,Xn
Risk Statements 
36/37/38-36-22
Safety Statements 
26-36/37/39
RIDADR 
UN 2920 8/3/PG II
HazardClass 
IRRITANT
PackingGroup 
II
HS Code 
2933399990
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1-ISOPROPYL-PIPERIDIN-4-YLAMINE Usage And Synthesis

Uses

1-Isopropylpiperidin-4-amine is used as a pharmaceutical intermediate compound for the preparation of antiviral compounds or small molecule bioactive inhibitors.

Synthesis

609804-23-1

127285-08-9

GENERAL METHOD: Compound I-5 (240 mg) was dissolved in hexafluoroisopropanol (HFIP, 8 mL) and 10% palladium/carbon (Pd/C, 120 mg) was added. The reaction mixture was stirred at room temperature for 20 h under hydrogen atmosphere (1 atm). Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated to give the yellow oily product I-6 (100 mg, 75% yield).

References

[1] European Journal of Medicinal Chemistry, 2017, vol. 132, p. 26 - 41
[2] Patent: EP1489078, 2004, A1. Location in patent: Page 130

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