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1-Isopropyl-piperidin-4-ylamine

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1-Isopropyl-piperidin-4-ylamine manufacturers

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;AKOS B016068
CAS:127285-08-9
MF:C8H18N2
MW:142.24
EINECS:
Product Categories:Heterocycles
Mol File:127285-08-9.mol
1-Isopropyl-piperidin-4-ylamine Structure
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
pka10.51±0.20(Predicted)
color Colorless to Almost colorless
InChIInChI=1S/C8H18N2/c1-7(2)10-5-3-8(9)4-6-10/h7-8H,3-6,9H2,1-2H3
InChIKeyZRQQXFMGYSOKDF-UHFFFAOYSA-N
SMILESN1(C(C)C)CCC(N)CC1
CAS DataBase Reference127285-08-9(CAS DataBase Reference)
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
MSDS Information
1-Isopropyl-piperidin-4-ylamine Usage And Synthesis
Uses1-Isopropylpiperidin-4-amine is used as a pharmaceutical intermediate compound for the preparation of antiviral compounds or small molecule bioactive inhibitors.
Synthesis
Carbamic acid, [1-(1-methylethyl)-4-piperidinyl]-, phenylmethyl ester (9CI)

609804-23-1

1-ISOPROPYL-PIPERIDIN-4-YLAMINE

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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