Substance
ID:311096
Names and Identifiers
IUPAC name
azetidine
IUPAC Traditional name
azetidine
Synonyms
Trimethylene imine杂氮环丁烷Azetidine氮杂环丁烷
Registration numbers
CAS Number
EC Number
Beilstein Number
MDL Number
PubChem SID
Properties
Physical Property
Refractive Index
n20/D 1.432(lit.)
Density
0.847 g/mL at 25 °C(lit.)
Flash Point
-21 °C
-5.8 °F
Boiling Point
61-62 °C(lit.)
Safety Information
GHS Signal Word
Danger
Storage Temperature
2-8°C
Packing Group
2
European Hazard Symbols
Corrosive (C)
Flammable (F)Personal Protective Equipment
Faceshields, full-face respirator (US), Gloves, Goggles, multi-purpose combination respirator cartridge (US)
Risk Statements
11-34
UN Number
2733
German water hazard class
3
GHS Precautionary statements
P210-P280-P305+P351+P338-P310
GHS Pictograms
Corrosive to metals, category 1
Skin corrosion, categories 1A,1B,1C
Serious eye damage, category 1
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
GHS Hazard statements
H225-H314
RID/ADR
UN 2733 3/PG 2
Safety Statements
16-26-36/37/39-45
MSDS Link
Hazard Class
3
Product Information
Purity
98%
Empirical Formula (Hill Notation)
C3H7N
Molecule Details
Application
Employed in a high yielding palladium-catalyzed cross-coupling with aryl bromides.1 Also used in a Ullmann type coupling with iodonitroflourenes.2
Packaging
1 g in ampule
100, 250 mg in ampule
Employed in a high yielding palladium-catalyzed cross-coupling with aryl bromides.1 Also used in a Ullmann type coupling with iodonitroflourenes.2
Packaging
1 g in ampule
100, 250 mg in ampule
Molecular Spectra
No Data Available
Click here to submit data
References
No Data Available
Click here to submit data