148289-52-5

Basic information

• Product Name: (2S,3R)-2-amino-1,3-(dibenzyloxy)-octadeca-4-ene
• Synonyms: (2S,3R)-2-amino-1,3-(dibenzyloxy)-octadeca-4-ene
• CAS NO: 148289-52-5
• Molecular Weight: 479.747
• Mol File: 148289-52-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (2S,3R)-2-amino-1,3-(dibenzyloxy)-octadeca-4-ene(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R)-2-amino-1,3-(dibenzyloxy)-octadeca-4-ene(148289-52-5)
• EPA Substance Registry System: (2S,3R)-2-amino-1,3-(dibenzyloxy)-octadeca-4-ene(148289-52-5)

Safety Data

• Hazardous Substances Data: 148289-52-5(Hazardous Substances Data)

Upstream product

• 603-35-0 triphenylphosphine 
• 137410-26-5 (2S,3R,4E)-2-azido-1,3-dibenzyloxyoctadeca-4-ene 
• 100-44-7 benzyl chloride 
• 16054-77-6 3,5-di-O-benzyl-D-xylofuranose 
• 41341-99-5 3,5-di-O-benzyl-1,2-O-isopropylidene-α-D-xylofuranose 
• 25791-20-2 (n-tetradecyl)triphenylphosphonium bromide 
• 112-71-0 1-Bromotetradecane 
• 148289-50-3 (2R,3R)-1,3-Di-O-benzyl-2-O-(methylsulfonyl)-4-octadecene-1,2,3-triol 
• 148289-49-0 (2R,3R)-1,3-Di-O-benzyl-4-octadecene-1,2,3-triol 

Downstream Products

• 148289-53-6 (2S,3R)-1,3-di-O-benzyl-2-(N-tetradecanoylamino)-4-octadecene-1,3-diol 
• 1053549-93-1 Acetic acid (R)-1-[(1S,2R)-2-hydroxy-1-((2S,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxymethyl)-heptadecylcarbamoyl]-tricosyl ester 
• 1053748-43-8 Acetic acid (R)-1-[(1S,2R)-2-hydroxy-1-((2S,3R,4S,5S,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxymethyl)-heptadecylcarbamoyl]-pentacosyl ester 
• 123-78-4 (2S,3R,4E)-2-amino-4-octadecene-1,3-diol 

Relevant articles and documents

Stereoselective synthesis of N,O,O,O-tetraacetyl-D-ribo-phytosphingosine, N,O,O-triacetyl-D-erythro-sphingosine and N,O,O-triacetyl sphingonine from a common chiral intermediate derived from D-mannitol

An efficient protocol for the stereoselective synthesis of tetraacetyl-D-ribo-hytosphingosine, triacetyl-D-erythro-sphingosine and triacetyl sphinganine has been devised from a common chiral intermediate derived from commercially available D-mannitol. The key steps involved are Sharpless epoxidation, Miyashita C(2) selective endo mode azide opening of 2,3-epoxy alcohol, and selective E-Wittig olefination. ARKAT-USA, Inc.