56599-87-2

Basic information

• Product Name: Hexadecanoic acid, 2-phenyl-1,3-dioxan-5-yl ester
• CAS NO: 56599-87-2
• Molecular Formula: C26H42O4
• Molecular Weight: 418.617
• Mol File: 56599-87-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Hexadecanoic acid, 2-phenyl-1,3-dioxan-5-yl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Hexadecanoic acid, 2-phenyl-1,3-dioxan-5-yl ester(56599-87-2)
• EPA Substance Registry System: Hexadecanoic acid, 2-phenyl-1,3-dioxan-5-yl ester(56599-87-2)

Safety Data

• Hazardous Substances Data: 56599-87-2(Hazardous Substances Data)

Upstream product

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

Downstream Products

• 23470-00-0 2-palmitoylglycerol 
• 65266-83-3 Hexadecanoic acid 2-(toluene-4-sulfonyloxy)-1-(toluene-4-sulfonyloxymethyl)-ethyl ester 
• 142-91-6 palmitic acid isopropyl ester 
• 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 articles and documents

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.