4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

Base Information

Chemical Name:4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione
CAS No.:312756-03-9
Molecular Formula:C₁₄H₁₆N₄O₂S₂
Molecular Weight:336.439
Hs Code.:

Synonyms:4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

Suppliers and Price of 4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

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 0 raw suppliers

Chemical Property of 4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

There total 2 articles about 4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione 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: 69.0%

: 110-91-8,99108-56-2
morpholine

: 1350301-74-4
5-(4-isothiocyanatophenyl)-2-methylsulfanyl-1,3,4-oxadiazole

: 312756-03-9
4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

Guidance literature:: In benzene; for 3h; Reflux;
DOI:10.1016/j.bmc.2011.09.038

Reference yield:

: 5-(4-isothiocyanatophenyl)-1,3,4-oxadiazole-2-thiol

: 312756-03-9
4-(5-methylsulfanyl-1,3,4-oxadiazol-2-yl)anilinomorpholinomethanethione

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / acetone / 2 h / 20 °C

2: benzene / 3 h / Reflux

With triethylamine; In acetone; benzene;
DOI:10.1016/j.bmc.2011.09.038