Azetidine hydrochloride

Names

[ Name ]:
Azetidine hydrochloride

[Synonym ]:
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

Biological Activity

[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

[ Storage condition ]:
Room temperature.

MSDS

Click to get detail MSDS

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%

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...