CHEBI:75131 - (1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol

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ChEBI Name (1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol
ChEBI ID CHEBI:75131
ChEBI ASCII Name (1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol
Definition An N-[1-hydroxy-3-(morpholin-4-yl)-1-phenylpropan-2-yl]hexadecanamide in which both stereocentres have S configuration.
Stars This entity has been manually annotated by the ChEBI Team.
Supplier Information
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Formula C29H50N2O3
Net Charge 0
Average Mass 474.71890
Monoisotopic Mass 474.38214
InChI InChI=1S/C29H50N2O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-17-20-28(32)30-27(25-31-21-23-34-24-22-31)29(33)26-18-15-14-16-19-26/h14-16,18-19,27,29,33H,2-13,17,20-25H2,1H3,(H,30,32)/t27-,29-/m0/s1
InChIKey OFBANDBMHLEMFA-YTMVLYRLSA-N
SMILES CCCCCCCCCCCCCCCC(=O)N[C@@H](CN1CCOCC1)[C@@H](O)c1ccccc1
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75131) is a N-[1-hydroxy-3-(morpholin-4-yl)-1-phenylpropan-2-yl]hexadecanamide (CHEBI:75125)
(1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75131) is enantiomer of (1R,2R)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75126)
Incoming DL-threo-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75132) has part (1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75131)
(1R,2R)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75126) is enantiomer of (1S,2S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (CHEBI:75131)
IUPAC Name
N-[(1S,2S)-1-hydroxy-3-(morpholin-4-yl)-1-phenylpropan-2-yl]hexadecanamide
Synonyms Sources
(1S,2S)-2-hexadecanoylamino-3-morpholino-1-phenylpropan-1-ol ChemIDplus
(1S,2S)-3-morpholino-2-palmitoylamino-1-phenylpropan-1-ol ChemIDplus
(1S,2S)-PPMP ChemIDplus
(1S,threo)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol ChemIDplus
(1S,threo)-PPMP ChemIDplus
(S,S)-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol ChemIDplus
(S,S)-PPMP ChemIDplus
L-threo-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol ChEBI
L-threo-PPMP ChEBI
N-[(1S,2S)-1-hydroxy-3-(morpholin-4-yl)-1-phenylpropan-2-yl]palmitamide ChEBI
N-[(1S,2S)-2-hydroxy-1-(4-morpholinylmethyl)-2-phenylethyl]hexadecanamide ChemIDplus
N-[(1S,2S)-2-hydroxy-1-(4-morpholinylmethyl)-2-phenylethyl]palmitamide ChEBI
Registry Number Type Source
7910702 Reaxys Registry Number Reaxys
Last Modified
23 August 2013
General Comment
2013-08-14 For synthesis, see Nishida, A., Sorimachi, H., Iwaida, M., Matsumizu, M., Kawate, T. and Nakagawa, M. (1998) Synlett, 389-390.