126568-85-2

Basic information

• Product Name: 3-O-lauroyl-2-O-benzyl-D-glcerol
• Synonyms: 3-O-lauroyl-2-O-benzyl-D-glcerol
• CAS NO: 126568-85-2
• Molecular Weight: 364.525
• Mol File: 126568-85-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-O-lauroyl-2-O-benzyl-D-glcerol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-O-lauroyl-2-O-benzyl-D-glcerol(126568-85-2)
• EPA Substance Registry System: 3-O-lauroyl-2-O-benzyl-D-glcerol(126568-85-2)

Safety Data

• Hazardous Substances Data: 126568-85-2(Hazardous Substances Data)

Upstream product

• 109429-01-8 (S)-2-(benzyloxy)-3-hydroxypropyl acetate 
• 91274-04-3 (R)-2-benzyloxy-3-trityloxy-propan-1-ol 
• 117009-43-5 (S)-1-O-acetyl-2-O-benzyl-3-O-tritylglycerol 
• 112-16-3 n-dodecanoyl chloride 
• 220446-52-6 2,5-dibenzyl-1,6-dilauroyl-D-mannitol 
• 17618-04-1 2,5-di-O-benzyl-D-mannitol 
• 126568-82-9 Dodecanoic acid (S)-2-benzyloxy-3-trityloxy-propyl ester 

Downstream Products

• 126568-93-2 (2S,4S,5R,6R)-4-Acetoxy-5-acetylamino-2-((S)-2-benzyloxy-3-dodecanoyloxy-propoxy)-6-((1S,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 126610-80-8 (2R,4S,5R,6R)-4-Acetoxy-5-acetylamino-2-((S)-2-benzyloxy-3-dodecanoyloxy-propoxy)-6-((1S,2R)-1,2,3-triacetoxy-propyl)-tetrahydro-pyran-2-carboxylic acid methyl ester 
• 1108727-87-2 3-O-lauroyl-2-O-benzyl-D-glycerol p-nitrobenzenesulfonate 
• 1108727-86-1 3-O-lauroyl-2-O-benzyl-D-glycerol p-bromobenzenesulfonate 
• 1108727-82-7 3-O-lauroyl-2-O-benzyl-D-glycerol p-methylbenzenesulfonate 
• 1108727-81-6 3-O-lauroyl-2-O-benzyl-D-glycerol benzenesulfonate 
• 1108727-85-0 3-O-lauroyl-2-O-benzyl-D-glycerol p-chlorobenzenesulfonate 
• 1108727-88-3 3-O-lauroyl-2-O-benzyl-D-glycerol methanesulfonate 
• 220446-56-0 2-benzyl-1-lauroyl-sn-glycero-3-[phospho-1-isopropylideneglycerol] methyl ester 

Relevant articles and documents

New 3-O-lauroyl-2-O-benzyl-glycerol sulfonate

The hydroxy groups of D-mannitol were protected by the formation of acetals and benzylethers and then 2-O-benzyl-D-glyceraldehyde dimethylacetal was prepared after the deprotection and oxygenolysis of the protected D-mannitol. In the presence of DCC and D

Neuraminic acid and related compounds. V. Syntheses of biologically active sialosyl-glycerol derivatives and galactosyl-glycerol derivative

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