78715-90-9

Basic information

• Product Name: 1-O-Benzoyl C2 CeraMide
• Synonyms: 1-O-Benzoyl C2 CeraMide;1-O-benzoyl Acetyl CeraMide;1-O-benzoyl N-Acetylsphingosine;1-O-benzoyl-N-[(1S,2R,3E)-2-hydroxy-1-(hydroxyMethyl)-3-heptadecen-1-yl]acetaMide;1-O-benzoyl-N-acetyl-D-sphingosine
• CAS NO: 78715-90-9
• Molecular Formula: C₂₇H₄₃NO₄
• Molecular Weight: 445.63462
• Product Categories: Fatty Acid Derivatives & Lipids;Glycerols;Inhibitors;Protein Kinase Inhibitors and Activators
• Mol File: 78715-90-9.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Solubility: Dichloromethane, Methanol
• CAS DataBase Reference: 1-O-Benzoyl C2 CeraMide(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-Benzoyl C2 CeraMide(78715-90-9)
• EPA Substance Registry System: 1-O-Benzoyl C2 CeraMide(78715-90-9)

Safety Data

• Hazardous Substances Data: 78715-90-9(Hazardous Substances Data)

Usage

Chemical Properties

Off-white Solid

Uses

C2 Ceramide (C262500) derivative.

Upstream product

• 78715-83-0 methyl (S)-2-phenyl-4,5-dihydrooxazole-4-carboxylate 
• 825-60-5 benzimidic acid ethyl ester 
• 78715-85-2 erythro-4-(1-hydroxy-2-hexadecenyl)-2-phenyl-Δ²-oxazoline 
• 78715-84-1 4-formyl-2-phenyl-Δ²-oxazoline 
• 765-13-9 pentadec-1-yne 
• 830-03-5 4-nitrophenol acetate 
• 78739-32-9 1-O-Benzoyl-D-erythro-C₁₈-sphingosine hydrochloride 

Downstream Products

• 2482-37-3 (2S,3R,4E)-2-acetamido-1,3-diacetoxyoctadec-4-ene 
• 3102-57-6 N-acetyl-D-erythro-sphingosine 

Relevant articles and documents

Useful Syntheses of erythro- and threo-N-Oleoyl-D-sphingosines (Ceramides) and Galactosylceramides (Cerebrosides) from L-Serine

The 4-(carbomethoxy)-2-phenyl-Δ2-oxazoline formed from L-serine provides the basis for a useful synthesis of ceramides and cerebrosides.The natural erythro configuration and its threo epimer are formed in equal amounts but are readily separated chromatographically, so that both epimers are available for experiments in which the properties of erythro and threo configurations are to be compared.The method produces the final cerebroside product on a scale of 100 mg or more.The optical purity of the product was shown to be close to 100percent.In addition to the threo epimer, other analogues of the natural cerebrosides with different chain le ngths and stereochemistries should be readily available by using the route developed.Such molecules are of interest to us for (13)C NMR and related studies of membrane organization.