Azetidine hydrochloride
Azetidine hydrochloride structure
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Common Name | Azetidine hydrochloride | ||
|---|---|---|---|---|
| CAS Number | 36520-39-5 | Molecular Weight | 93.56 | |
| Density | N/A | Boiling Point | 103.8ºC at 760 mmHg | |
| Molecular Formula | C3H8ClN | Melting Point | >300 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 152 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Practical syntheses of N-substituted 3-hydroxyazetidines and 4-hydroxypiperidines by hydroxylation with Sphingomonas sp. HXN-200.
Org. Lett. 4 , 1859-1862, (2002) [reaction: see text] Hydroxylation of N-substituted azetidines 11 and 12 and piperidines 15-19 with Sphingomonas sp. HXN-200 gave 91-98% of the corresponding 3-hydroxyazetidines 13 and 14 and 4-hydroxypiperidines 20-24, respectively, with high activity and ex... |
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Domino formation of enamines--intramolecular cyclizations to 1-aminotetralins from γ-arylallene aldehydes and amines.
Org. Lett. 16(20) , 5438-41, (2014) 1,5-/1,6-Allenals conjugated to an aromatic ring undergo a cyclization, in the presence of an amine, that leads to tricyclic compounds including the 1-aminotetralin scaffold. This domino process combines the in situ formation of the enamine and the cyclizatio... |
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Synthesis and biological evaluation of a novel phenyl substituted sydnone series as potential antitumor agents.
Bioorg. Med. Chem. Lett. 13 , 2899-2901, (2003) A series of compounds containing an N-(4'-substituted-3'-nitrophenyl)sydnone moiety with potential antitumor activity was prepared based on active analogues. The rationale behind the design of these compounds is presented along with the 4-step synthetic route... |
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Synthesis of ornithine lactams via diastereoselective photocyclization of 2-amino-4-oxo-4-phenyl-butanoyl amines. Lindemann U, et al.
Tetrahedron Asymmetry 9(24) , 4459-73, (1998)
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