95603-89-7

Upstream product

• 7769-79-1 2-aminohexadecanoic acid 
• 108-05-4 vinyl acetate 
• 764-67-0 2-hydroxypalmitic acid 

Downstream Products

• 87384-99-4 (R)-2-Hydroxy-hexadecanoic acid [(3E,7Z)-(1S,2R)-2-hydroxy-1-((3R,4S,5S,6R)-3,4,5-trihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxymethyl)-heptadeca-3,7-dienyl]-amide 
• 34839-06-0 (R)-2-Hydroxy-hexadecanoic acid ((1S,2R)-2-hydroxy-1-hydroxymethyl-heptadecyl)-amide 
• 100992-30-1 (4E,8E,2S,3S,2'R)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8,-sphingadienine 
• 100924-04-7 (4E,8E,2S,3R,2'R)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-9-methyl-4,8-sphingadienine 
• 88642-46-0 1-O-(β-D-glucopyranosyl)-(2S,3R,4E,8E)-2-[(2'R)-2'-(hydroxyhexadecanoyl)amido]-9-methyl-4,8-octadecadiene-1,3-diol 
• 100933-63-9 (4E,8E,2S,3R,2'R)-N-2'-hydroxyhexadecanoyl-1-O-(tetra-O-acetyl-β-D-glucopyranosyl)-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 100924-07-0 (4E,8E,2S,3R,2'R)-N-2'-hydroxyhexadecanoyl-1-O-β-D-glucopyranosyl-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 100924-05-8 (4E,8E,2S,3R,2'R)-N-2'-acetoxyhexadecanoyl-1-O-benzoyl-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 100924-06-9 (4E,8E,2S,3R,2'R)-N-2'-hydroxyhexadecanoyl-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 115538-45-9 Benzoic acid (2E,6Z)-(R)-1-[(S)-1-((R)-2-acetoxy-hexadecanoylamino)-2-hydroxy-ethyl]-hexadeca-2,6-dienyl ester 
• 115648-52-7 Benzoic acid (2E,6Z)-(S)-1-[(R)-1-((R)-2-acetoxy-hexadecanoylamino)-2-hydroxy-ethyl]-hexadeca-2,6-dienyl ester 
• 115589-64-5 Acetic acid (R)-1-((3E,7Z)-(1R,2S)-2-hydroxy-1-trityloxymethyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester 
• 115523-77-8 Acetic acid (R)-1-((3E,7Z)-(1S,2R)-2-hydroxy-1-trityloxymethyl-heptadeca-3,7-dienylcarbamoyl)-pentadecyl ester 
• 115074-93-6 soya-cerebroside II 

Relevant academic research and scientific papers

SYNTHESIS 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, AND ITS (2R,3S)-ISOMER

A synthesis of the natural enantiomer as well as its diastereomer of the title compound was accomplished, confirming the structure proposed for the fruiting-inducing cerebroside of Schizophyllum commune.