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1,2-Epoxy-9-decen
96%
Synonym(e):
(7-Octenyl)-oxiran
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25 ML
152,00 €
About This Item
Empirische Formel (Hill-System):
C10H18O
CAS-Nummer:
Molekulargewicht:
154.25
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Qualitätsniveau
Assay
96%
Form
liquid
Brechungsindex
n20/D 1.442 (lit.)
Dichte
0.842 g/mL at 25 °C (lit.)
Funktionelle Gruppe
allyl
ether
SMILES String
C=CCCCCCCC1CO1
InChI
1S/C10H18O/c1-2-3-4-5-6-7-8-10-9-11-10/h2,10H,1,3-9H2
InChIKey
FCZHJHKCOZGQJZ-UHFFFAOYSA-N
Verwandte Kategorien
Allgemeine Beschreibung
1,2-Epoxy-9-decene is an unsaturated epoxide. Hydrogenation of the C=C bond of 1,2-epoxy-9-decene over palladium nanoparticles, namely PdOAc,N has been reported.[1]
Signalwort
Danger
H-Sätze
Gefahreneinstufungen
Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Lagerklassenschlüssel
10 - Combustible liquids
WGK
WGK 3
Flammpunkt (°F)
172.4 °F - closed cup
Flammpunkt (°C)
78 °C - closed cup
Persönliche Schutzausrüstung
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Claire Jeanquartier et al.
Langmuir : the ACS journal of surfaces and colloids, 24(24), 13957-13961 (2009-04-11)
A versatile two-step method has been developed that allows linking of biomolecules covalently to hydrogen-terminated group-IV semiconductors by means of epoxy-alkenes. First, the terminal C==C double bond of the alkene forms a covalent bond with the silicon, germanium, or diamond
Yuan Lu et al.
Biomacromolecules, 14(10), 3589-3598 (2013-08-22)
A series of amphiphilic nitric oxide (NO)-releasing poly(amidoamine) (PAMAM) dendrimers with different exterior functionalities were synthesized by a ring-opening reaction between primary amines on the dendrimer and propylene oxide (PO), 1,2-epoxy-9-decene (ED), or a ratio of the two, followed by
Reactivity versus Stability of Oxiranes under Palladium-Catalyzed Reductive Conditions.
Thiery E, et al.
European Journal of Organic Chemistry, 2009(7), 961-985 (2009)
Alexandra Shakun et al.
Polymers, 11(7) (2019-07-03)
Detonation nanodiamonds, also known as ultradispersed diamonds, possess versatile chemically active surfaces, which can be adjusted to improve their interaction with elastomers. Such improvements can result in decreased dielectric and viscous losses of the composites without compromising other in-rubber properties
Yuan Lu et al.
Chemistry of materials : a publication of the American Chemical Society, 23(18), 4227-4233 (2011-11-05)
Structurally diverse secondary amine-functionalized poly(propylene imine) (PPI) dendrimers capable of tunable nitric oxide (NO) release were synthesized in a straightforward, one-step manner using ring-opening or conjugate-addition reactions with propylene oxide (PO), styrene oxide (SO), acrylonitrile (ACN), poly(ethylene glycol) methyl ether
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