111279
4-Penten-1-ol
99%
Synonym(e):
2-Allyl-ethylalkohol
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Empfohlene Produkte
Qualitätsniveau
Assay
99%
Brechungsindex
n20/D 1.429 (lit.)
bp
134-137 °C (lit.)
Dichte
0.834 g/mL at 25 °C (lit.)
Funktionelle Gruppe
allyl
hydroxyl
SMILES String
OCCCC=C
InChI
1S/C5H10O/c1-2-3-4-5-6/h2,6H,1,3-5H2
InChIKey
LQAVWYMTUMSFBE-UHFFFAOYSA-N
Suchen Sie nach ähnlichen Produkten? Aufrufen Leitfaden zum Produktvergleich
Allgemeine Beschreibung
4-penten-1-ol forms ester bond at the C terminus of the linear peptide in solution with HATU as coupling agent.
Anwendung
4-Penten-1-ol can be used as a reactant to prepare sulfamate ester by reacting with chlorosulfonyl isocycanate (142662).The derived ester undergoes an enantioselective intramolecular azridination reaction in the presence of Cu catalyst. 4-Penten-1-ol can also be used to study the epoxidation of olefins with oxo-diperoxo tungstate(VI) complex as catalyst and bicarbonate as co-catalyst.
Hier finden Sie alle aktuellen Versionen:
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Kunden haben sich ebenfalls angesehen
Highly efficient epoxidation method of olefins with hydrogen peroxide as terminal oxidant, bicarbonate as a co-catalyst and oxodiperoxo molybdenum(VI) complex as catalyst.
New. J. Chem., 30(3), 479-489 (2006)
Enantioselective Intramolecular Copper-Catalyzed Aziridination of Sulfamates
Synthesis, 1251-1251 (2007)
Journal of molecular modeling, 17(6), 1251-1257 (2010-08-17)
The mechanism of phenylselenoetherification of pent-4-en-1-ol using some bases (pyridine, triethylamine, quinoline, 2,2'-bipyridine) as catalyst was examined through studies of kinetics of the cyclization, by UV-VIS spectrophotometry. It was demonstrated that the intramolecular cyclization is facilitated in the presence of
Bioorganic & medicinal chemistry, 16(13), 6580-6588 (2008-05-30)
In the recent years, we focused our attention on the cyclodepsipeptide Jaspamide 1, an interesting marine metabolite, possessing a potent inhibitory activity against breast and prostate cancer, as a consequence of its ability to disrupt actin cytoskeleton dynamics. Although its
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung.