69502-95-0

Basic information

• Product Name: 3-Octadecene-1,2-diol
• Synonyms: 3-Octadecene-1,2-diol
• CAS NO: 69502-95-0
• Molecular Weight: 0
• Mol File: 69502-95-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 3-Octadecene-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Octadecene-1,2-diol(69502-95-0)
• EPA Substance Registry System: 3-Octadecene-1,2-diol(69502-95-0)

Safety Data

• Hazardous Substances Data: 69502-95-0(Hazardous Substances Data)

Upstream product

• 111394-70-8 (2S)-1,2-di-O-isopropylidene-3-octadecene-1,2-diol 
• 111394-70-8 (2S)-1,2-O-isopropyliden-octadec-3(Z)-ene-1,2-diol 
• 1944-80-5 pentadecyltriphenylphosphonium bromide 
• 629-72-1 pentadecyl bromide 
• 97818-08-1 Pentadecylidene-triphenyl-λ⁵-phosphane 
• 22566-56-9 ethyl 2-oxooctadec-3-ynoate 
• 629-74-3 hexadec-1-yne 
• 1352742-30-3 (2R)-ethyl 2-hydroxyoctadec-3-ynoate 
• 131606-83-2 (R)-1,2-cyclohexylidenedioxyoctadec-3-yne 
• 131606-85-4 (R)-3-octadec-3-yne-1,2-diol 
• 131606-82-1 (S)-1,2-cyclohexylidenedioxyoctadec-3-yne 
• 131606-84-3 (S)-3-octadec-3-yne-1,2-diol 

Downstream Products

• 111394-79-7 (Z)-(R)-Octadec-3-ene-1,2-diol 
• 111394-80-0 Benzoic acid (Z)-(S)-2-((S)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-octadec-3-enyl ester 
• 111466-48-9 D-arabino-phytosphingosine 
• 111394-72-0 (2S)-1-benzoyloxy-3-octadecene-2-ol 
• 112025-51-1 (2S)-1,2-dibenzoyloxy-3-octadecene 

Relevant articles and documents

Total synthesis of symbioramide: A flexible approach for the efficient preparation of structural isomers

A concise, enantioselective total synthesis of symbioramide, starting from simple achiral compounds and racemic α-amino-β-keto ester derivatives is reported. This highly flexible strategy allowed the efficient preparation of seven structural isomers of the natural product as well. The synthesis relies on a convergent route that involves the efficient stereoselective reduction of a α-keto-β-yne ester, and the dynamic kinetic resolution of an α-amino-β-keto ester through ruthenium-mediated asymmetric hydrogenation. Copyright

Total Synthesis of Symbioramide, a Novel Ca(2+)-ATPase Activator from Symbiodinium sp.

The first total synthesis of symbioramide 1 has been accomplished by the coupling of D-erythro-dihydrosphingosine with an unusual, chiral α-hydroxy-β,γ-unsaturated fatty acid prepared from L-ascorbic acid, and simultaneously established the complete stereostructure of 1 to be (2S,2'R,3R,3'E)-N-(2'-hydroxyoctadec-3'-enoyl)dihydrosphingosine.

CHEMISTRY OF AYURVEDIC CRUDE DRUGS - VII GUGGULU (RESIN FROM COMMIPHORA MUKUL) - 6 ABSOLUTE STEREOCHEMISTRY OF GUGGULTETROLS

With a view to elucidating the stereochemistry of guggultetrols, components of saponified Commiphora mukul resin, D-lyxo-, L-ribo-, and L-xylo-octadecane-1,2,3,4-tetrols have been synthesised by two different routes.One method starts with D-glyceraldehyde