84415-90-7

Basic information

• Product Name: 1-Propanol, 3-(hexadecyloxy)-2-(phenylmethoxy)-, (R)-
• CAS NO: 84415-90-7
• Molecular Formula: C26H46O3
• Molecular Weight: 406.649
• Mol File: 84415-90-7.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 1-Propanol, 3-(hexadecyloxy)-2-(phenylmethoxy)-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Propanol, 3-(hexadecyloxy)-2-(phenylmethoxy)-, (R)-(84415-90-7)
• EPA Substance Registry System: 1-Propanol, 3-(hexadecyloxy)-2-(phenylmethoxy)-, (R)-(84415-90-7)

Safety Data

• Hazardous Substances Data: 84415-90-7(Hazardous Substances Data)

Upstream product

• 96960-87-1 2-O-benzyl-1-O-hexadecyl D-glyceraldehyde 
• 36653-82-4 1-Hexadecanol 
• 20779-14-0 methanesulfonic acid hexadecyl ester 
• 100-51-6 benzyl alcohol 
• 122564-58-3 3-O-hexadecyl-2-O-benzyl-sn-glycerol 1-O-p-toluenesulfonate 
• 119944-30-8 3‐hexadecyloxy‐2R‐hydroxyl propyl‐1‐p‐toluene sulphonate 
• 17674-16-7 benzyl triflate 
• 114935-21-6 2,5-di-O-benzyl-1,6-bis-O-(4-methoxy-benzyl)-D-mannitol 
• 114935-18-1 2,5-di-O-benzyl-1,3(R):4,6(R)-bis-O-(4-methoxy-benzylidene)-D-mannitol 
• 114935-25-0 (S)-2-benzyloxy-3-(4-methoxy-benzyloxy)-propan-1-ol 
• 100-39-0 benzyl bromide 
• 120019-37-6 3-hexadecyloxy-2R-hydroxypropyl 1-para-toluenesulphonate 
• 84379-59-9 2-O-benzyl-1-O-hexadecyl-3,4-O-isopropylidene-L-threitol 
• 84379-61-3 2-O-benzyl-1-O-hexadecyl-L-threitol 

Downstream Products

• 96998-53-7 3-O-hexadecyl-2-O-benzyl-sn-glycero-1-phosphocholine 
• 96022-71-8 2-O-Benzyl-3-O-hexadecyl-1-O-<2,3,6-tri-O-acetyl-4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-β-D-glucopyranosyl>-sn-glycerin 
• 78119-19-4 2-hydroxy-3-(hexadecyloxy)-propyl 2-trimethylammonioethyl phosphate 
• 90130-75-9 3-O-hexadecyl-2-lyso-sn-glycero-1-phosphocholine 

Relevant articles and documents

Synthesis of optically pure (R)-and (S)-1-alkyl-2-acyl- glycerophosphocholine (in German)

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NOVEL ENANTIOSELECTIVE SYNTHESIS OF PLATELET ACTIVATING FACTOR AND ITS ENANTIOMER VIA RING OPENING OF GLYCIDYL TOSYLATE WITH 1-HEXADECANOL

(2R)-and(2S)-Glycidyl tosylates 3 and 3' were used to synthesize platelet activating factor 1 and its enantiomer 2 in very high optical purity via the ring-opened ether-linked glycerol tosylate 4 and 4'

Stereoselective Synthesis of Long-chain 1-O-(β-D-Maltosyl)-3-O-alkyl-sn-glycerols (Alkyl Glyceryl Ether Lysoglycolipids)

The synthesis of long-chain 2-O-benzyl-3-O-alkyl-sn-glycerols 5 was improved, making these compounds easily accessible for glycosylation experiments.Glycosylation with α-acetobromomaltose following a modified Koenings-Knorr procedure after removal of the protective groups yielded the title compound 9 in good yields.These compounds represent examples of alkyl glyceryl ether lysoglycolipids.Some properties of these amphiphilic compounds with a nonionic carbohydrate head-group differ not much (critical micell concentration, hemolytic activity), other properties differ very much (antitumor efficiency) from the properties of the analogous compounds with a zwitterionic phosphorylcholine head-group.