Azetidine

Modify Date: 2024-01-03 08:02:38

Azetidine Structure
Azetidine structure
Common Name Azetidine
CAS Number 503-29-7 Molecular Weight 57.094
Density 0.9±0.1 g/cm3 Boiling Point 64.9±8.0 °C at 760 mmHg
Molecular Formula C3H7N Melting Point N/A
MSDS Chinese USA Flash Point -23.6±16.5 °C
Symbol GHS02 GHS05
GHS02, GHS05
Signal Word Danger

 Names

Name azetidine
Synonym More Synonyms

 Chemical & Physical Properties

Density 0.9±0.1 g/cm3
Boiling Point 64.9±8.0 °C at 760 mmHg
Molecular Formula C3H7N
Molecular Weight 57.094
Flash Point -23.6±16.5 °C
Exact Mass 57.057850
PSA 12.03000
LogP -0.20
Vapour Pressure 161.5±0.1 mmHg at 25°C
Index of Refraction 1.426
Storage condition 2-8°C
Water Solubility miscible

 Safety Information

Symbol GHS02 GHS05
GHS02, GHS05
Signal Word Danger
Hazard Statements H225-H314
Precautionary Statements P210-P280-P305 + P351 + P338-P310
Personal Protective Equipment Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US)
Hazard Codes F: Flammable;C: Corrosive;
Risk Phrases R11;R34
Safety Phrases S16-S26-S36/37/39-S45
RIDADR UN 2733 3/PG 2
WGK Germany 3
Packaging Group I
Hazard Class 3.1
HS Code 29339990

 Synthetic Route

 Customs

HS Code 2933990090
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 Articles31

More Articles
Synthesis from D-altrose of (5R,6R,7R,8S)-5,7-dihydroxy-8-hydroxymethylconidine and 2,4-dideoxy-2,4-imino-D-glucitol, azetidine analogues of swainsonine and 1,4-dideoxy-1,4-imino-D-mannitol.

Org. Lett. 14(16) , 4174-7, (2012)

Ring closure of a 3,5-di-O-triflate derived from D-altrose with benzylamine allowed the formation of both monocyclic and bicyclic azetidine analogues of swainsonine.

Identification of spirocyclic piperidine-azetidine inverse agonists of the ghrelin receptor.

Bioorg. Med. Chem. Lett. 22(13) , 4281-7, (2012)

The discovery of spirocyclic piperidine-azetidine inverse agonists of the ghrelin receptor is described. The characterization and redressing of the issues associated with these compounds is detailed. ...

Complex N-heterocycle synthesis via iron-catalyzed, direct C-H bond amination.

Science 340(6132) , 591-5, (2013)

The manipulation of traditionally unreactive functional groups is of paramount importance in modern chemical synthesis. We have developed an iron-dipyrrinato catalyst that leverages the reactivity of ...

 Synonyms

Azetidine
MFCD00005165
Trimethylenimine
EINECS 207-963-8
1,3-Propylenimine
Azetidin
trimethyleneimine
Azacyclobutane
UNII-37S883XDWR
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