85-4029-60　(S)-(-)-Propylene Oxide 1g　CAS No:16088-62-3　288395

特徴

• (S)-Methyloxirane is a reactant that has been used in the synthesis of (-)-Pyrenophorol, the macrolide dilactone Pyrenophorol was originally isolated from Byssochlamys niveah and Stemphylium radicinum. Pyrenophorol was moderately active against the fungus Microbotryum violaceum. It is an anti-fungal antibiotic produced by the plant pathogenic fungi Pyrenophora avenue and Stemphylium radicinum, which is closely related structurally to (-)-Pyrenophorol.
• (S)-(−)-Propylene oxide undergoes ring-opening upon treating with nucleophiles such as Grignard reagents or organolithium compounds to yield corresponding secondary alcohols.[1][2]
•  It can be used in the synthesis of ligands to prepare of Pb(II) based coordination nets for the fabrication of white light-emitting diode materials.[1]
•  It is a key starting material for the total synthesis of arenolide[2] and (+)-aspicilin.[3]
• Synonyms:(2S)-Methyloxirane; (S)-(-)-Propylene Oxide; (-)-Methyloxirane; (-)-Propylene Oxide; (2S)-2-Methyloxirane; (2S)-Methyloxirane; (S)-(-)-Methyloxirane; (S)-(-)-Propene Oxide; (S)-(-)-Propylene oxide; (S)-2-Methyloxirane; (S)-Methyloxirane; (S)-Propene Oxide; (S)-Propylene oxide; S-(-)-1,2-Epoxypropane; l-Propylene Oxide
• Molecular Formula:C₃H₆O
• Molecular Weight:58.08
• Appearance:Liquid
• Purity:≥98% (GC)
• Refractive Index:n20/D 1.366 (lit.)
• Boiling Point:33-34 °C (lit.)
• Density:0.829g/ml at 20°C (lit.)
• Storage and Stability:Store at -20°C. Heat Sensitive. For maximum recovery of product, centrifuge the original vial prior to removing the cap.