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Merck
CN

C110507

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24892345
EC Number:
206-010-3
Beilstein/REAXYS Number:
103543
MDL number:
MFCD00005164
Assay:
99%
Form:
crystals

Key Documents

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Product Name

Cyclooctene oxide, 99%

InChI key

MELPJGOMEMRMPL-UHFFFAOYSA-N

InChI

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

SMILES string

C1CCCC2OC2CC1

assay

99%

form

crystals

bp

55 °C/5 mmHg (lit.)

mp

53-56 °C (lit.)

Quality Level

100

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Related Categories

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

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

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 2

flash_point_f

145.4 °F - closed cup

flash_point_c

63 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB5655
STBK6613
STBJ9676
STBH3982
STBG8832

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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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