Sisaustricin

Base Information

Chemical Name:Sisaustricin
CAS No.:59170-06-8
Molecular Formula:C₅H₉NOS
Molecular Weight:131.199
Hs Code.:
UNII:6GL59KY9NZ
Nikkaji Number:J903.847G

Synonyms:Sisaustricin;Sisaustricine;(+)-Sisaustricin;6GL59KY9NZ;4-Ethyl-2-oxazolidinethione, (+)-;2-Oxazolidinethione, 4-ethyl-, (4R)-;59170-06-8;UNII-6GL59KY9NZ;AKOS006352537

Suppliers and Price of Sisaustricin

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 Sisaustricin

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:131.04048508
Heavy Atom Count:8
Complexity:105

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC1COC(=S)N1
Isomeric SMILES:CC[C@@H]1COC(=S)N1

Technology Process of Sisaustricin

There total 4 articles about Sisaustricin 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: 52.0%

: 96-20-8,13054-87-0
2-aminobutanol

: MoO₂S₄C₂N₂C₄H₁₂

: 13997-20-1,59170-06-8,94238-48-9
4-ethyl-1,3-oxazolidine-2-thione

Guidance literature:: In toluene; for 1.5h; Heating;
DOI:10.1016/j.tetlet.2007.07.212

Reference yield:

: 96-20-8,13054-87-0
2-aminobutanol

: 75-15-0,12122-00-8
carbon disulfide

: 13997-20-1,59170-06-8,94238-48-9
4-ethyl-1,3-oxazolidine-2-thione

Guidance literature:: 2-aminobutanol; carbon disulfide; With triethylamine; In methanol; at 0 - 20 ℃; for 0.5h;

With dihydrogen peroxide; In methanol; water; Reflux;
DOI:10.1002/jhet.862