78739-32-9

Basic information

• Product Name: 1-O-Benzoyl-D-erythro-C₁₈-sphingosine hydrochloride
• Synonyms: 1-O-Benzoyl-D-erythro-C₁₈-sphingosine hydrochloride
• CAS NO: 78739-32-9
• Molecular Weight: 440.066
• Mol File: 78739-32-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-O-Benzoyl-D-erythro-C₁₈-sphingosine hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1-O-Benzoyl-D-erythro-C₁₈-sphingosine hydrochloride(78739-32-9)
• EPA Substance Registry System: 1-O-Benzoyl-D-erythro-C₁₈-sphingosine hydrochloride(78739-32-9)

Safety Data

• Hazardous Substances Data: 78739-32-9(Hazardous Substances Data)

Upstream product

• 15890-72-9 laurylmagnesium bromide 
• 173531-24-3 (4S,1'S,2'R)-4-(1',2'-Epoxybut-3'-enyl)-2-phenyl-4,5-dihydrooxazole 
• 78715-85-2 erythro-4-(1-hydroxy-2-hexadecenyl)-2-phenyl-Δ²-oxazoline 
• 78715-83-0 methyl (S)-2-phenyl-4,5-dihydrooxazole-4-carboxylate 
• 825-60-5 benzimidic acid ethyl ester 
• 78715-84-1 4-formyl-2-phenyl-Δ²-oxazoline 
• 765-13-9 pentadec-1-yne 
• 173531-22-1 Methanesulfonic acid (1R,2S,3R)-2,4-dihydroxy-3-methanesulfonyloxy-1-((S)-2-phenyl-4,5-dihydro-oxazol-4-yl)-butyl ester 
• 173531-23-2 (1'R,2'R,4S)-1'-Methylsulfonyloxy-1'-(2-phenyl-4,5-dihydrooxazol-4-yl)but-3'-en-2'-ol 

Downstream Products

• 78715-88-5 N-oleoyl-3-O-(tert-butyldiphenylsilyl)-D-sphingosine (erythro epimer) 
• 5966-28-9 N-oleoyl-D-sphingosine (erythro form) 
• 78715-87-4 N-oleoyl-1-O-benzoyl-3-O-(tert-butyldiphenylsilyl)-D-sphingosine (erythro form) 
• 2482-37-3 (2S,3R,4E)-2-acetamido-1,3-diacetoxyoctadec-4-ene 
• 3102-57-6 N-acetyl-D-erythro-sphingosine 
• 139757-37-2 N-Benzoyl-D-erythro-C₁₈-sphingosine 
• 123-78-4 (2S,3R,4E)-2-amino-4-octadecene-1,3-diol 
• 177547-63-6 Benzoic acid (E)-(2S,3R)-2-ethoxycarbonylamino-3-hydroxy-octadec-4-enyl ester 
• 78715-90-9 erythro-N-acetyl-1-O-benzoylsphingosine 
• 78715-86-3 erythro-1-O-benzoylceramide 

Relevant articles and documents

Efficient stereocontrolled synthesis of D-erythro-sphingosine from N-benzoyl-D-glucosamine

D-erythro-Sphingosine is synthesized from N-benzoyl-D-glucosamine 2 in a highly regio- and stereo-controlled manner. The key features in the synthesis involve the efficient conversion of compound 2 into the vinyl epoxide 10 and the subsequent SN2′-type reaction with a Grignard reagent in the presence of CuCN to afford the 1-O,2-N-protected sphingosine 11.