ChemicalBook--->CAS DataBase List--->127285-08-9

127285-08-9

127285-08-9 Structure

127285-08-9 Structure
IdentificationMore
[Name]

1-ISOPROPYL-PIPERIDIN-4-YLAMINE
[CAS]

127285-08-9
[Synonyms]

1-ISOPROPYLPIPERIDIN-4-AMINE
1-ISOPROPYL-PIPERIDIN-4-YLAMINE
4-AMINO-1-ISOPROPYL PIPERIDINE
AKOS B016068
ART-CHEM-BB B016068
N-ISO-PROPYL-4-AMINO-PIPERIDINE
TIMTEC-BB SBB009390
N-Iso-proppyl-4-amino-piperidine
[Molecular Formula]

C8H18N2
[MDL Number]

MFCD03411606
[Molecular Weight]

142.24
[MOL File]

127285-08-9.mol
Chemical PropertiesBack Directory
[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)
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 .
[RIDADR ]

UN 2920 8/3/PG II
[HazardClass ]

IRRITANT
[PackingGroup ]

II
[HS Code ]

2933399990
Hazard InformationBack Directory
[Uses]

1-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
Spectrum DetailBack Directory
[Spectrum Detail]

1-ISOPROPYL-PIPERIDIN-4-YLAMINE(127285-08-9)1HNMR
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