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Chemical Structure| 201036-16-0 Chemical Structure| 201036-16-0

Structure of DPyPE
CAS No.: 201036-16-0

Chemical Structure| 201036-16-0

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Synonyms: 1,2-Diphytanoyl-sn-glycero-3-PE; 1,2-Diphytanoyl-sn-glycero-3-Phosphoethanolamine; 4ME 16:0 PE

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Product Details of [ 201036-16-0 ]

CAS No. :201036-16-0
Formula : C45H90NO8P
M.W : 804.17
SMILES Code : [C@@H](OC(=O)CC(C)CCCC(C)CCCC(C)CCCC(C)C)(COC(=O)CC(C)CCCC(C)CCCC(C)CCCC(C)C)COP(O)(=O)OCCN
Synonyms :
1,2-Diphytanoyl-sn-glycero-3-PE; 1,2-Diphytanoyl-sn-glycero-3-Phosphoethanolamine; 4ME 16:0 PE
English Name :(2R)-3-(((2-Aminoethoxy)(hydroxy)phosphoryl)oxy)propane-1,2-diyl bis(3,7,11,15-tetramethylhexadecanoate)
MDL No. :MFCD00674318

Safety of [ 201036-16-0 ]

Application In Synthesis of [ 201036-16-0 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 201036-16-0 ]

[ 201036-16-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 32607-05-9 ]
  • [ 201036-16-0 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: Py / CHCl3 2: Zn / aq. acetic acid; diethyl ether 3: (i) Py, CHCl3, (ii) Zn, AcOH, Et2O
  • 2
  • [ 39028-25-6 ]
  • [ 201036-16-0 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
In dimethyl sulfoxide at 40℃; for 0.5h; 2.2.2. Covalent modification General procedure: Lipids (20 nmoL) were derivatized with IB-NHS ester by reacting 1:2 ratio (lipid: IB-NHS ester) in 100 mL 1:1 borate buffer (pH 8.5):organic solvent (DMSO) for 30 min at 40 °C in a water bath. After cooling, water (0.5 mL) and chloroform (0.5 mL) were sequentially added to the solution. The chloroform phase was then collected and diluted in methanol to a final lipid concentration of 5 mM prior to negative ion ESI-MS experiments. Reaction yields were estimated to be 90-100% for PE lipids and 30-50% for PS lipids (see Fig. S-5).
 

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