![]() Azetidine structure
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Common Name | Azetidine | ||
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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 |
Signal Word | Danger |
Purity | Quantity | Budget | Inquiry |
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Name | azetidine |
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Synonym | More Synonyms |
Density | 0.9±0.1 g/cm3 |
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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 |
Symbol |
![]() ![]() GHS02, GHS05 |
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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 |
~0% |
Literature: Ohishi, Takeshi; Nishiura, Masayoshi; Hou, Zhaomin Angewandte Chemie - International Edition, 2008 , vol. 47, # 31 p. 5792 - 5795 |
~39% |
Literature: Correa, Arkaitz; Martin, Ruben Journal of the American Chemical Society, 2009 , vol. 131, # 44 p. 15974 - 15975 |
~98% |
Literature: Wiles, Charlotte; Watts, Paul; Haswell, Stephen J. Tetrahedron Letters, 2006 , vol. 47, # 30 p. 5261 - 5264 |
HS Code | 2933990090 |
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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% |
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. |
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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. ... |
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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 ... |
Azetidine |
MFCD00005165 |
Trimethylenimine |
EINECS 207-963-8 |
1,3-Propylenimine |
Azetidin |
trimethyleneimine |
Azacyclobutane |
UNII-37S883XDWR |