C102504
Cyclohexene oxide
98%
Synonym(s):
1,2-Epoxycyclohexane, 7-Oxabicyclo[4.1.0]heptane
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About This Item
Empirical Formula (Hill Notation):
C6H10O
CAS Number:
Molecular Weight:
98.14
UNSPSC Code:
12162002
NACRES:
NA.23
PubChem Substance ID:
EC Number:
206-007-7
Beilstein/REAXYS Number:
383568
MDL number:
assay
98%
form
liquid
autoignition temp.
703 °F
expl. lim.
12.36 %
refractive index
n20/D 1.452 (lit.)
bp
129-130 °C (lit.)
density
0.97 g/mL at 25 °C (lit.)
SMILES string
C1CCC2OC2C1
InChI
1S/C6H10O/c1-2-4-6-5(3-1)7-6/h5-6H,1-4H2
InChI key
ZWAJLVLEBYIOTI-UHFFFAOYSA-N
Application
- Polymeric carbon nitride with internal np homojunctions for efficient photocatalytic CO2 reduction coupled with cyclohexene oxidation: This study focuses on the use of cyclohexene oxide in the context of photocatalytic CO2 reduction, highlighting the application of polymeric carbon nitride as a catalyst. The process shows how cyclohexene oxide can be efficiently converted in a coupled reaction that also addresses environmental concerns through CO2 reduction (W Zhen et al., 2021).
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Muta. 2 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Regulatory Information
危险化学品
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Highly active dizinc catalyst for the copolymerization of carbon dioxide and cyclohexene oxide at one atmosphere pressure.
Michael R Kember et al.
Angewandte Chemie (International ed. in English), 48(5), 931-933 (2008-12-31)
Benedetta Mennucci et al.
The Journal of organic chemistry, 72(18), 6680-6691 (2007-08-09)
The optical rotatory power of some natural cyclohexene oxides, such as (+)-chaloxone, 1, (+)-epiepoformine, 2, (+)-epoformine, 3, (+)-epoxidone, 5, (-)-sphaeropsidone, 6, (-)-episphaeropsidone, 7, and the synthetic compound (+)-epitheobroxide, 4, has been calculated by means of the TDDFT/B3LYP method using the
Yoshiyuki Igawa et al.
Toxicology and applied pharmacology, 234(3), 361-369 (2008-11-26)
The polycyclic aromatic hydrocarbon 7, 12-dimethylbenz[a]anthracene, (DMBA), targets and destroys all follicle types in rat and mouse ovaries. DMBA requires bioactivation to DMBA-3,4-diol-1,2-epoxide for ovotoxicity via formation of the intermediate, DMBA-3,4-diol (catalyzed by microsomal epoxide hydrolase; mEH). mEH was shown
Global Trade Item Number
| SKU | GTIN |
|---|---|
| C102504-25ML | 04061833460443 |
| C102504-500ML | 04061833460450 |
| C102504-100ML | 04061833460436 |