CAS 36520-39-5|Azetidine hydrochloride
Introduction：Basic information about CAS 36520-39-5|Azetidine hydrochloride, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
| Common Name | Azetidine hydrochloride | ||
|---|---|---|---|
| CAS Number | 36520-39-5 | Molecular Weight | 93.56 |
| Density | / | Boiling Point | 103.8ºC at 760 mmHg |
| Molecular Formula | C3H8ClN | Melting Point | >300 °C(lit.) |
| MSDS | ChineseUSA | Flash Point | 152 °C |
| Symbol | GHS07 | Signal Word | Warning |
Names
| Name | Azetidine hydrochloride |
|---|---|
| Synonym | More Synonyms |
Azetidine hydrochloride BiologicalActivity
| Description | Azetidine hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. |
|---|---|
| Related Catalog | Research Areas >>Others |
Chemical & Physical Properties
| Boiling Point | 103.8ºC at 760 mmHg |
|---|---|
| Melting Point | >300 °C(lit.) |
| Molecular Formula | C3H8ClN |
| Molecular Weight | 93.56 |
| Flash Point | 152 °C |
| Exact Mass | 93.034531 |
| PSA | 12.03000 |
| LogP | 1.11050 |
| InChIKey | HGQULGDOROIPJN-UHFFFAOYSA-N |
| SMILES | C1CNC1.Cl |
| Storage condition | Room temperature. |
Safety Information
| Symbol | GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi:Irritant; |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2933990090 |
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% |
Articles4
More Articles| 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-hydrox... | |
| 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 combi... | |
| 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 c... |
Synonyms
| Azetidine, hydrochloride (1:1) |
| azetadine hydrochloride |
| Azetidinhydrochlorid |
| AZETIDINE HCL |
| azetidine monohydrochloride |
| Azacyclobutane Hydrochloride |
| Azetidine hydrochloride (1:1) |
| TRIMETHYLENEIMINE HYDROCHLORIDE |
| azetidinium chloride |
| hydrochloride salt of azetidine |
| azetidine HCl salt |
| EINECS 207-963-8 |
| TriMethyleniMine Hydrochloride |
| MFCD00191762 |
| 1,3-PropyleniMine Hydrochloride |
| Tetrahydro-azete Hydrochloride |
