ChemicalBook--->CAS DataBase List--->4396-01-4

4396-01-4

4396-01-4 Structure

4396-01-4 Structure
IdentificationBack Directory
[Name]

pelletierine
[CAS]

4396-01-4
[Synonyms]

pelletierine
isopelletierine
1-piperidin-2-ylacetone
1-(2-Piperidinyl)acetone
2-(2-Oxopropyl)piperidine
1-(2-Piperidyl)-2-propanone
1-piperidin-2-ylpropan-2-one
1-(2-Piperidinyl)-2-propanone
2-Propanone, 1-(2-piperidinyl)-
1-piperidin-2-ylacetone (SALTDATA: FREE)
1-piperidin-2-ylacetone(SALTDATA: 0.15H2O)
1-Piperidin-2-ylacetone DISCONTINUED. Please see B449984.
2-Acetonylpiperidinepunicineisopelletierine, (.+/-.)-pelletierine
[EINECS(EC#)]

224-523-0
[Molecular Formula]

C8H15NO
[MDL Number]

MFCD01459222
[MOL File]

4396-01-4.mol
[Molecular Weight]

141.21
Chemical PropertiesBack Directory
[Melting point ]

130-132 °C
[Boiling point ]

195 °C
[density ]

0.918±0.06 g/cm3(Predicted)
[storage temp. ]

Hygroscopic, -20°C Freezer, Under inert atmosphere
[solubility ]

Chloroform (Slightly), Ethyl Acetate (Slightly)
[form ]

Oil
[pka]

pK1:9.45 (15°C)
[color ]

Colourless to Light Yellow
[Stability:]

Hygroscopic
Hazard InformationBack Directory
[Description]

An alkaloid of this name was discovered by Tanret but when this alkaloid was shown to be (±)-pelletierine, the name was adopted for this particular base isolated from Punica granatum. The alkaloid is an oily liquid which yields a number of well crystalline salts and derivative: the hydrochloride, m.p. 143°C; hydrobromide, m.p. 149°C; picrate, m.p. 147 -8°C and the picrolonate, m.p. 185-6°C. The N-acetyl derivative is an oily liquid, b.p. 110-5°C/0.I mm while the N-benzoyl compound is crystalline with m.p. 72-4°C. The alkaloid may be prepared by the demethylation of methylisopelletierine, the action being revers_x0002_ible.
[Definition]

ChEBI: Pelletierine is a citraconoyl group.
[References]

Tanret., Compt. rend., 88, 716 (1879) Tanret., ibid, 90, 696 (1880) Hesse., Rev. trav. Chim., 52, 1005 (1919) Hess, Littman., Annalen, 494, 7 (1932) Wibaut, Kloppenburg, Beets., Rev. trav. Chim., 63, 134 (1944) Anet, Hughes, Ritchie., Nature, 164, 50 I (1949) Galinovsky, Branchetti, Vogl.,Monatsh., 84, 1221 (1953) Galinovsky, Hollinger., ibid, 85, 1012 (1954) Wibaut, Hirschel., Rev. trav. Chim., 75,225 (1956)
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