Substance

ID:720349

Names and Identifiers
IUPAC Traditional name
6-oxabicyclo 3.1.0 hexane
IUPAC name
6-oxabicyclo[3.1.0]hexane
Synonyms
Cyclopentene oxide氧化环戊烯6-Oxabicyclo[3.1.0]hexaneEpoxycyclopentane
Registration numbers
MDL Number
Beilstein Number
CAS Number
EC Number
Properties
Physical Property
Refractive Index
1.4340
Density
0.965
Boiling Point
101-102°C
Flash Point
10°C(50°F)
Safety Information
GHS Hazard statements
H225-H341-H315-H319-H335
Safety Statements
16-23-26-36/37
GHS Pictograms
GHS02
Flammable gases, category 1
Flammable aerosols, categories 1,2
Flammable liquids, categories 1,2,3
Self-reactive substances and mixtures, Types B,C,D,E,F
Pyrophoric liquids, category 1
Pyrophoric solids, category 1
Self-heating substances and mixtures
Substances and mixtures, which in contact with water, emit flammable gases, categories 1,2,3
Organic peroxides, Types B,C,D,E,F
GHS08
Respiratory sensitization, category 1
Germ cell mutagenicity, categories 1A,1B,2
Carcinogenicity, categories 1A,1B,2
Reproductive toxicity, categories 1A,1B,2
Specific Target Organ Toxicity – Single exposure, categories 1,2
Specific Target Organ Toxicity – Repeated exposure, categories 1,2
Aspiration Hazard, category 1
GHS07
Acute toxicity (oral, dermal, inhalation), category 4
Skin irritation, category 2
Eye irritation, category 2
Skin sensitisation, category 1
Specific Target Organ Toxicity – Single exposure, category 3
European Hazard Symbols
Irritant Irritant (Xi)
Flammable Flammable (F)
Hazard Class
3
UN Number
UN1993
GHS Precautionary statements
P210-P261-P280H-P305+P351+P338
Risk Statements
11-36/37/38-68
Packing Group
III
RTECS
RN8935000
TSCA Listed
Product Information
Purity
97%
Molecule Details
No Data Available
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Molecular Spectra
No Data Available
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References
• Base-induced isomerization can give 2-cyclopentenol or cyclopentanone depending on the conditions. For discussion of the mechanism, see: J. Org. Chem., 61, 820 (1996), and references therein. Review of the rearrangement of epoxides to allylic alcohols: Org. React., 29, 345 (1983).