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410829

Sigma-Aldrich

1,2-Epoxy-9-decen

96%

Synonym(e):

(7-Octenyl)-oxiran

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About This Item

Empirische Formel (Hill-System):
C10H18O
CAS-Nummer:
85721-25-1
Molekulargewicht:
154.25
EG-Nummer:
288-437-5
MDL-Nummer:
MFCD00069427
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24865706
NACRES:
NA.22

Assay

96%

Form

liquid

Brechungsindex

n20/D 1.442 (lit.)

Dichte

0.842 g/mL at 25 °C (lit.)

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

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.

Piktogramme

CorrosionExclamation mark
GHS05,GHS07

Signalwort

Danger

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

Reactivity versus Stability of Oxiranes under Palladium-Catalyzed Reductive Conditions.
Thiery E, et al.
European Journal of Organic Chemistry, 2009(7), 961-985 (2009)
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
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
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

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