2011762-82-4

Basic information

• Product Name: N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]-18,18,18-d₃-octadecanamid
• CAS NO: 2011762-82-4
• Molecular Weight: 568.941
• Mol File: 2011762-82-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]-18,18,18-d₃-octadecanamid(CAS DataBase Reference)
• NIST Chemistry Reference: N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]-18,18,18-d₃-octadecanamid(2011762-82-4)
• EPA Substance Registry System: N-[(2S,3R,4E)-1,3-dihydroxyoctadec-4-en-2-yl]-18,18,18-d₃-octadecanamid(2011762-82-4)

Safety Data

• Hazardous Substances Data: 2011762-82-4(Hazardous Substances Data)

Upstream product

• 34957-73-8 methyl 9-hydroxynonanoate 
• 2104-19-0 azelaic monomethyl ester 
• 123-78-4 (2S,3R,4E)-2-amino-4-octadecene-1,3-diol 
• 62163-39-7 18,18,18-d₃-octadecanoic acid 
• 1219799-20-8 1-bromo-9,9,9-d₃-nonane 
• 1732-10-1 Dimethyl azelate 
• 55695-90-4 2-(9-bromononyloxy)tetrahydropyran 
• 98847-01-9 9-<(tetrahydro-2H-pyran-2-yl)oxy>nonyl methanesulfonate 
• 123-99-9 azelaic acid 
• 98847-00-8 9-<(2H-tetrahydropyran-2-yl)oxy>nonan-1-ol 
• 75949-34-7 methyl 9-[(tetrahydro-2H-pyran-2-yl)oxy]nonanoate 
• 17660-51-4 deuterated octadecanoic acid 

Relevant articles and documents

Synthesis of ceramides NS and NP with perdeuterated and specifically ω deuterated N-acyl residues

The synthesis of 12 deuterated ceramides with either a deuteration at the last carbon atom of the amide bound fatty acid or a perdeuterated fatty acid chain is described. The ceramides were prepared starting from sphingosine or phytosphingosine and ω deuterated or perdeuterated fatty acids with PyBOP as activating agent in high yields. For the synthesis of the specifically deuterated fatty acids, dicarboxylic acids were transformed into ω deuterated alkyl bromide, which was chain elongated with blocked ω bromo alcohols by copper catalyzed Grignard coupling. Oxidation of regenerated alcohol function yields the ω deuterated fatty acids.