56599-87-2

Upstream product

• 57-10-3 1-hexadecylcarboxylic acid 
• 1708-40-3 2-phenyl-[1,3]dioxan-5-ol 
• 100-52-7 benzaldehyde 

Downstream Products

• 65266-83-3 Hexadecanoic acid 2-(toluene-4-sulfonyloxy)-1-(toluene-4-sulfonyloxymethyl)-ethyl ester 
• 142-91-6 palmitic acid isopropyl ester 
• 23470-00-0 2-palmitoylglycerol 
• 572920-49-1 1-O-tert-butyldiphenylsilyl-2-O-palmitoyl-rac-glycero-3-phosphocholine 
• 572920-36-6 1-O-benzyl-2-O-palmitoyl-rac-glycero-3-phosphocholine 
• 572920-56-0 1-O-benzyl-3-O-palmitoyl-rac-glycero-2-phosphocholine 
• 572920-43-5 1-O-tert-butyldiphenylsilyl-2-O-palmitoyl-rac-glycerol 
• 22128-35-4 1-O-benzyl-2-O-palmitoyl-rac-glycerol 
• 17364-18-0 1-palmitoyllysophosphatidylcholine 
• 1487-51-0 1-O-benzyl-3-O-palmitoyl-rac-glycerol 

Relevant academic research and scientific papers

Functional acylglycerides

The present invention relates to the field of human and animal nutrition, and in particular to certain novel compositions of conjugated linoleic acids (CLA). In particular, the present invention relates certain isomers of conjugated linoleic acids at eith

Synthesis of 1-lyso-2-palmitoyl-rac-glycero-3-phosphocholine and its regioisomers and structural elucidation by NMR spectroscopy and FAB tandem mass spectrometry

Three regioisomers of a naturally occurring lysophosphatidylcholine were chemically synthesized from glycerol. The phosphocholine moiety of the molecule was introduced by sequentially reacting with ethylene chlorophosphite, bromine, water, and trimethyl amine. Removal of a silyl protecting group of the hydroxyl group in the glycerol backbone was achieved without any accompanying acyl migration in the final stage of the synthesis by using NBS in a dimethyl sulfoxide-water cosolvent system. Structures of all regioisomers were compared by NMR spectroscopy and FAB tandem mass spectrometry.