281069
Azetidine
98%
Synonym(s):
Trimethylene imine
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About This Item
Empirical Formula (Hill Notation):
C3H7N
CAS Number:
Molecular Weight:
57.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-963-8
Beilstein/REAXYS Number:
102384
MDL number:
Assay:
98%
Form:
liquid
Quality Level
assay
98%
form
liquid
refractive index
n20/D 1.432 (lit.)
bp
61-62 °C (lit.)
density
0.847 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
C1CNC1
InChI
1S/C3H7N/c1-2-4-3-1/h4H,1-3H2
InChI key
HONIICLYMWZJFZ-UHFFFAOYSA-N
Related Categories
General description
Phototransformations of azetidine radical cations in freonic matrices under the action of light with λ = 436nm has been investigated. The IR spectrum of azetidine in solid argon matrices has been measured.
Application
Azetidine was employed in:
- a high yielding palladium-catalyzed cross-coupling raection with aryl bromides
- Ullmann type coupling reaction with iodonitroflourenes
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
-4.0 °F
flash_point_c
-20 °C
ppe
Faceshields, Gloves, Goggles
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Phototransformations of azetidine radical cations stabilized in freonic matrices.
Sorokin ID, et al.
High Energy Chemistry, 48(3), 180-184 (2014)
Synthesis, 243-243 (2007)
Experimental and computational studies of the structure and vibrational spectra of azetidine derivatives.
Thompson CA, et al.
Journal of Molecular Structure, 491(1), 67-80 (1999)
Synthesis, 3245-3245 (2006)
Younghue Han et al.
Journal of medicinal chemistry, 55(18), 8188-8192 (2012-09-04)
Novel azetidines based on the 3-aryl-3-oxypropylamine scaffold were designed, synthesized, and evaluated as TRIs. Reduction of 1 followed by Swern oxidation and then Grignard reaction gave 3. The alkylation of 3 provided the corresponding azetidine derivatives 6, of which the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 281069-250MG | 04061826214602 |
| 281069-1G | 04061838135223 |
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