1-(Diphenylmethyl)azetidine-2-thione

Base Information

Chemical Name:1-(Diphenylmethyl)azetidine-2-thione
CAS No.:88047-73-8
Molecular Formula:C16H15NS
Molecular Weight:253.368
Hs Code.:
DSSTox Substance ID:DTXSID40516150
Wikidata:Q82377433

Synonyms:1-(Diphenylmethyl)azetidine-2-thione;88047-73-8;DTXSID40516150

Suppliers and Price of 1-(Diphenylmethyl)azetidine-2-thione

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 1-(Diphenylmethyl)azetidine-2-thione

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:253.09252066
Heavy Atom Count:18
Complexity:272

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN(C1=S)C(C2=CC=CC=C2)C3=CC=CC=C3

Technology Process of 1-(Diphenylmethyl)azetidine-2-thione

There total 3 articles about 1-(Diphenylmethyl)azetidine-2-thione 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: 92.0%

: (1-Benzhydryl-azetidin-2-ylidene)-dimethyl-ammonium; perchlorate

: 88047-73-8
1-benzhydrylazetidin-2-thione

Guidance literature:: With sodium hydrogensulfide; In acetone;
DOI:10.1039/c39830000818

Reference yield: 65.0%

: 65219-08-1
1-(diphenylmethyl)azetidin-2-one

: 88047-73-8
1-benzhydrylazetidin-2-thione

Guidance literature:: With Lawessons reagent; In tetrahydrofuran; Heating;
DOI:10.1055/s-2006-942452

Reference yield:

: 776-74-9
Bromodiphenylmethane

: 88047-73-8
1-benzhydrylazetidin-2-thione

Guidance literature:: Multi-step reaction with 2 steps

1: 11 percent / KOH; 18-crown-6 / benzene / 4 h / 20 °C

2: 65 percent / Lawesson's reagent / tetrahydrofuran / Heating

With Lawessons reagent; potassium hydroxide; 18-crown-6 ether; In tetrahydrofuran; benzene;
DOI:10.1055/s-2006-942452