Azetidine, dihydrochloride

Base Information

Chemical Name:Azetidine, dihydrochloride
CAS No.:78797-58-7
Molecular Formula:C₃H₇N*ClH
Molecular Weight:93.5562
Hs Code.:

Synonyms:

Suppliers and Price of Azetidine, dihydrochloride

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of Azetidine, dihydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Azetidine, dihydrochloride

There total 6 articles about Azetidine, dihydrochloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

: O-tert-butyl azetidine-1-carbothioate

: 78797-58-7,78797-59-8,78797-62-3,36520-39-5,65546-09-0
azetidine hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether; at 20 ℃; for 1h;
DOI:10.1021/ol503441d

Reference yield: 98.0%

: 1-[Bis-(4-methoxy-phenyl)-methyl]-azetidine

: 78797-58-7,78797-59-8,78797-62-3,36520-39-5,65546-09-0
azetidine hydrochloride

Guidance literature:: With hydrogenchloride; for 14h; Heating;
DOI:10.3987/R-1986-09-2467

Reference yield: 85.0%

: 109-77-3
malononitrile

: 78797-58-7,78797-59-8,78797-62-3,36520-39-5,65546-09-0
azetidine hydrochloride

Guidance literature:: malononitrile; With C₄₆H₁₇₈O₄₁Si₄₂; titanium(IV)isopropoxide; In toluene; at 100 ℃; for 24h; Inert atmosphere;

With hydrogenchloride; water; In toluene; at 20 ℃; for 4h; chemoselective reaction; Inert atmosphere;
DOI:10.1016/j.tet.2013.11.101