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C110507

Sigma-Aldrich

Cyclooctene oxide

99%

Synonym(s):

9-Oxabicyclo[6.1.0]nonane, Epoxycyclooctane

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About This Item

Empirical Formula (Hill Notation):
C8H14O
CAS Number:
286-62-4
Molecular Weight:
126.20
Beilstein:
103543
EC Number:
206-010-3
MDL number:
MFCD00005164
UNSPSC Code:
12352100
PubChem Substance ID:
24892345
NACRES:
NA.22

Assay

99%

form

crystals

bp

55 °C/5 mmHg (lit.)

mp

53-56 °C (lit.)

SMILES string

C1CCCC2OC2CC1

InChI

1S/C8H14O/c1-2-4-6-8-7(9-8)5-3-1/h7-8H,1-6H2

InChI key

MELPJGOMEMRMPL-UHFFFAOYSA-N

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Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Statements

H228,H302,H315,H319

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 2

Flash Point(F)

145.4 °F - closed cup

Flash Point(C)

63 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Bo Tang et al.
Chemistry, an Asian journal, 14(23), 4375-4382 (2019-10-28)
The efficient chemical conversion of carbon dioxide (CO2 ) into value-added fine chemicals is an intriguing but challenging route in sustainable chemistry. Herein, a hollow-structured bimetallic zeolitic imidazole framework composed of Zn and Co as metal centers (H-ZnCo-ZIF) has been
Yun Wang et al.
Materials (Basel, Switzerland), 12(20) (2019-10-12)
Catalyzed organic solvent-free (ep)oxidation were achieved using H3PM12O40 (M = Mo or W) complexes ionically grafted on APTES-functionalized nano-silica beads obtained from straightforward method (APTES = aminopropyltriethoxysilane). Those catalysts have been extensively analyzed through morphological studies (Dynamic Light Scattering (DLS)

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