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Merck

281069

Azetidine

98%

Synonym(s):

Trimethylene imine

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About This Item

Empirical Formula (Hill Notation):
C3H7N
CAS Number:
503-29-7
Molecular Weight:
57.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24856966
EC Number:
207-963-8
Beilstein/REAXYS Number:
102384
MDL number:
MFCD00005165
Assay:
98%
Form:
liquid

Key Documents

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InChI key

HONIICLYMWZJFZ-UHFFFAOYSA-N

InChI

1S/C3H7N/c1-2-4-3-1/h4H,1-3H2

SMILES string

C1CNC1

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

Quality Level

100

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

pictograms

FlameCorrosion
GHS02,GHS05

signalword

Danger

hcodes

H225,H314

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

Group 4: Flammable liquids + Type 1 petroleums + Hazardous rank II + Water insoluble liquid

fsl

281069-1G: + 281069-VAR: + 281069-BULK: + 281069-100MG: + 281069-250MG:

jan

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8744
STBK4235
STBJ1922
STBH6592
STBG0071V

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Synthesis, 243-243 (2007)
Synthesis, 3245-3245 (2006)
Phototransformations of azetidine radical cations stabilized in freonic matrices.
Sorokin ID, et al.
High Energy Chemistry, 48(3), 180-184 (2014)
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)
Niamh M O'Boyle et al.
European journal of medicinal chemistry, 46(9), 4595-4607 (2011-08-16)
The structure-activity relationships of antiproliferative β-lactams, focusing on modifications at the 4-position of the β-lactam ring, is described. Synthesis of this series of compounds was achieved utilizing the Staudinger and Reformatsky reactions. The antiproliferative activity was assessed in MCF-7 cells
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