Weight | 691.972 g/mol |
---|---|
Formula | C37H74NO8P |
Hydrogen Acceptors | 8 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 37 |
923-61-5 (923-61-5)
DPPE · DHPE · dipalmitoyl phosphatidylethanolamine
Score:
#1673 in Physics
,
#5158 in Chemistry
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- Organometallic molecular wires and other nanoscale-sized devices: An approach using the organoiron (dppe)Cp*Fe building block (Coordination Chemistry Reviews, 1998)
- Elemental Carbon Chain Bridging Two Iron Centers: Syntheses and Spectroscopic Properties of [Cp*(dppe)Fe-C4-FeCp*(dppe)]n+.cntdot.n[PF6]-. X-ray Crystal Structure of the Mixed Valence Complex (n = 1) (Journal of the American Chemical Society, 1995)
- Relative metal-hydrogen, -oxygen, -nitrogen, and -carbon bond strengths for organoruthenium and organoplatinum compounds; equilibrium studies of Cp*(PMe3)2RuX and (DPPE)MePtX systems (Journal of the American Chemical Society, 1987)
- Syntheses, structures, and spectro-electrochemistry of {Cp*(PP)Ru}CCCC{Ru(PP)Cp*} (PP = dppm, dppe) and their mono- and dications (Organometallics, 2003)
- NiCl2(dppe)-Catalyzed Cross-Coupling of Aryl Mesylates, Arenesulfonates, and Halides with Arylboronic Acids (Journal of Organic Chemistry, 2004)
- Influence of ligands and anions on the rate of carbon monoxide insertion into palladium-methyl bonds in the complexes (P-P)Pd(CH3)Cl and [(P-P)Pd(CH3)(L)]+SO3CF3- (P-P = dppe, dppp, dppb, dppf; L = CH3CN, PPh3) (Organometallics, 1992)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - DPPE
- DHPE
- dipalmitoyl phosphatidylethanolamine
- 1,2-dipalmitoyl-sn-glycero-3-phosphoethanolamine
- 1,2-dipalmitoyl-3-phosphatidylethanolamine
- phosphatidylethanolamine dipalmitoate
- dipalmitoyl cephalin
- 1,2-dipalmitoyl-rac-glycerophosphoethanolamine
- 1,2-dipalmitoyl-3-phosphatidylethanolamine, (R)-isomer
- 1,2-dipalmitoyl-3-phosphatidylethanolamine, (+-)-isomer
- 1,2-dihexadecyl-sn-glycero-3-phosphoethanolamine
- 1,2-dipalmitoyl-3-phosphatidylethanolamine, ion(1-)
-
SMILESCCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCCN)OC(=O)CCCCCCCCCCCCCCC
-
InChIKeySLKDGVPOSSLUAI-UHFFFAOYSA-N
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Synthesis
Palmitoyl chloride
+
Reactant
(O-acylation)
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