105243-34-3

Basic information

• Product Name: (4E,8E,2S,3R)-N-hexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine
• CAS NO: 105243-34-3
• Molecular Weight: 654.03
• Mol File: 105243-34-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (4E,8E,2S,3R)-N-hexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine(CAS DataBase Reference)
• NIST Chemistry Reference: (4E,8E,2S,3R)-N-hexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine(105243-34-3)
• EPA Substance Registry System: (4E,8E,2S,3R)-N-hexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine(105243-34-3)

Safety Data

• Hazardous Substances Data: 105243-34-3(Hazardous Substances Data)

Upstream product

• 57-10-3 1-hexadecylcarboxylic acid 
• 100924-01-4 (2'E,6'E,4S,1'R)-4-(1'-hydroxy-7'-methyl-2',6'-hexadecadienyl)-2-phenyl-1,3-oxazolin-2-ene 
• 100923-98-6 (E)-6-methyl-pentadec-5-en-1-yne 
• 78715-84-1 4-formyl-2-phenyl-Δ²-oxazoline 
• 1492-30-4 4-nitrophenyl palmitate 
• 100933-62-8 1-O-benzoylsphingadienine*HCl 

Relevant articles and documents

Synthesis and Biological Activity of the Isomers and Analogs of (4E,8E,2S,3R,2'R)-N-2'-Hydroxyhexadecanoyl-9-methyl-4,8-sphingadienine, the Ceramide Portion of the Fruiting-inducing Cerebroside in a Basidiomycete Schizophyllum commune

The title compounds were synthesized by employing 2-aminohexadecanoic acid and serine as the chiral sources, and served for an assay of fruiting-inducing activity on Schizophyllum commune.The structure-bioactivity relationship among closely related synthetic ceramides is discussed.