113773-89-0

Basic information

• Product Name: cerebroside
• CAS NO: 113773-89-0
• Molecular Weight: 756.117
• Mol File: 113773-89-0.mol
• Article Data: 1

Chemical Properties

• Melting Point: 187-190 °C
• Boiling Point: 890.6±65.0 °C(Predicted)
• Density: 1.08±0.1 g/cm3(Predicted)
• CAS DataBase Reference: cerebroside(CAS DataBase Reference)
• NIST Chemistry Reference: cerebroside(113773-89-0)
• EPA Substance Registry System: cerebroside(113773-89-0)

Safety Data

• Hazardous Substances Data: 113773-89-0(Hazardous Substances Data)

Upstream product

• 160226-27-7 (R)-2-acetoxyoctadecanoic acid 
• 26633-48-7 (2R)-2-hydroxyoctadecanoic acid 
• 160147-96-6 (2S,3R,4E,8E)-N-trifluoroacetyl-1-O-(tetra-O-acetyl-β-D-glucopyranosyl)-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 160147-97-7 (2S,3R,4E,8E)-1-O-(β-D-glucopyranosyl)-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 160147-94-4 (2S,3R,4E,8E)-N-trifluoroacetyl-1-O-trityl-9-methyl-4,8-sphingadienine 
• 160147-95-5 (2S,3R,4E,8E)-N-trifluoroacetyl-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 
• 160147-91-1 p-nitrophenyl (R)-2-acetoxyoctadecanoate 
• 160147-93-3 (2S,3R,4E,8E)-N-trifluoroacetyl-9-methyl-4,8-sphingadienine 
• 160226-28-8 (2S,3R,4E,8E)-9-methyl-4,8-sphingadienine 
• 57-11-4 stearic acid 
• 142-94-9 2-bromostearic acid 
• 160147-98-8 (2S,2'R,3R,4E,8E)-N-2'-acetoxyoctadecanoyl-1-O-(β-D-glucopyranosyl)-3-O-(t-butyldiphenylsilyl)-9-methyl-4,8-sphingadienine 

Downstream Products

• 100896-30-8 (2R)-2-hydroxyoctadecanoic acid methyl ester 
• 26633-48-7 (2R)-2-hydroxyoctadecanoic acid 

Relevant articles and documents

Synthesis of (2S,2'R,3R,4E,8E)-N-2'-Hydroxyoctadecanoyl-1-O-(β-D-glucopyranosyl)-9-methyl-4,8-sphingadienine (Pen III), a Cerebroside Isolated from Penicillium funiculosum as the Fruiting Inducer against Schizophyllum commune

(2S,2'R,3R,4E,8E)-N-2'-Hydroxyoctadecanoyl-1-O-(β-D-glucopyranosyl)-9-methyl-4,8-sphingadienine (Pen III), a cerebroside isolated from Penicillium funiculosum A-1 as the fruiting inducer against Basidiomycete Schizophyllum commune, was synthesized by starting from D-glucose, L-serine, homoprenyl acetate and stearic acid.