131606-98-9

Basic information

• Product Name: methyl (2'R,3'E)-2'-hydroxyoctadec-3'-enoate
• Synonyms: methyl (2'R,3'E)-2'-hydroxyoctadec-3'-enoate
• CAS NO: 131606-98-9
• Molecular Weight: 312.493
• Mol File: 131606-98-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: methyl (2'R,3'E)-2'-hydroxyoctadec-3'-enoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (2'R,3'E)-2'-hydroxyoctadec-3'-enoate(131606-98-9)
• EPA Substance Registry System: methyl (2'R,3'E)-2'-hydroxyoctadec-3'-enoate(131606-98-9)

Safety Data

• Hazardous Substances Data: 131606-98-9(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 150178-55-5 (1R,2S,5R)-5-methyl-2-(1-methyl-1-phenylethyl)cyclohexyl (2R,3E)-2-hydroxy-3-octadecenoate 
• 150178-56-6 (1R,2S)-2-phenyl-1-cyclohexyl (2R,3E)-2-hydroxy-3-octadecenoate 
• 1363377-89-2 1-O-β-D-glucopyranosyl-(2S,3S,4E,9E)-2-[(2R,3E)-2-hydroxyoctadec-3-enoylamino]-10-methyl-octadeca-4,9-diene-1,3-diol 
• 1283114-63-5 (2R,3E)-2-hydroxy-N-[(2S,3R,4E,8Z)-1-β-D-glucopyranosyloxy-3-hydroxyhexadeca-4,8-dien-2-yl]octadec-3-enamide 
• 1184182-50-0 (2R,3E)-2-hydroxy-N-[(2S,3R,4E,8Z)-1-β-D-glucopyranosyloxy-3-hydroxyoctadec-4,8-dien-2-yl]octadec-3-enamide 
• 1184182-48-6 (2R,3E)-2-hydroxy-N-[(2S,3R,4E,8E)-1-β-D-glucopyranosyloxy-3-hydroxy-9-methylheptadec-4,8-dien-2-yl]octadec-3-enamide 
• 1184182-47-5 (2R,3E)-2-hydroxy-N-[(2S,3R,4E)-1-β-D-glucopyranosyloxy-3-hydroxy-9-methylene-8-oxooctadec-4-en-2-yl]octadec-3-enamide 
• 1083079-89-3 1-O-(α-D-glucopyranosyl)-(2S,3R,4E,8E,10E)-2-[(2'R,3'E)-2'-hydroxyoctadec-3'-enoylamino]-9-methyloctadeca-4,8,10-triene-1,3-diol 

Relevant articles and documents

Ceramide and cerebrosides from the octocoral sarcophyton ehrenbergi

Chemical investigation of the octocoral Sarcophyton ehrenbergi, collected at the Dongsha Islands, Taiwan, has led to the isolation of a known ceramide (1) and two new cerebrosides, sarcoehrenosides A (2)andB(4), along with three known cerebrosides (3, 5,

Flavusides A and B, antibacterial cerebrosides from the marine-derived fungus Aspergillus flavus

Flavusides A (1) and B (2), two new antibacterial cerebroside derivatives, and the previously described phomaligol A (3), kojic acid (4), methyl kojic acid (5), and dimethyl kojic acid (6) have been isolated from the extract of a marine isolate of the fungus Aspergillus flavus. The structure and absolute stereochemistry of two cerebrosides were assigned on the basis of NMR and Tandem FAB-MS/MS experiments. Compounds 1, 2, and 3 exhibited a mild antibacterial activity against Staphylococcus aureus, methicillin-resistant S. aureus, and multidrug-resistant S. aureus. The minimum inhibitory concentration (MIC) values for each strain are as follows: compounds 1 and 2 showed 15.6 μg/ml for S. aureus and 31.2 μg/ml for methicillin-resistant S. aureus and multidrug-resistant S. aureus, and compound 3 exhibited 31.2 μg/ml for S. aureus and methicillin-resistant S. aureus and 62.5 μg/ml for multidrug-resistant S. aureus.

Diastereoselective Reduction of Chiral β,γ-Unsaturated α-Oxo Esters. Asymmetric Synthesis of the Fatty Acid Moiety of Symbioramide

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