(5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-2-thione

Base Information

Chemical Name:(5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-2-thione
CAS No.:80102-30-3
Molecular Formula:C7H12N2S2
Molecular Weight:188.318
Hs Code.:
DSSTox Substance ID:DTXSID80508973

Synonyms:80102-30-3;DTXSID80508973;(5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-2-thione

Suppliers and Price of (5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-2-thione

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 1 raw suppliers

Chemical Property of (5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-2-thione

Chemical Property:

XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:188.04419074
Heavy Atom Count:11
Complexity:221

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1(C(=NC)SC(=S)N1C)C

Technology Process of (5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-2-thione

There total 2 articles about (5Z)-3,4,4-Trimethyl-5-(methylimino)-1,3-thiazolidine-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:

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

: 2273-39-4
2-methylamino-2-methylpropanenitrile

: 74-89-5
methylamine

: 80102-30-3
3,4,4-trimethyl-5-methyliminothiazolidine-2-thione

: 19355-69-2
2-amino-2-cyanopropane

Guidance literature:: for 24h; Heating;

Reference yield:

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

: 2273-39-4
2-methylamino-2-methylpropanenitrile

: 80102-30-3
3,4,4-trimethyl-5-methyliminothiazolidine-2-thione

: 20513-25-1
5,5-dimethylimidazolidine-2,4-dithione

: 80102-31-4
imino-5 trimethyl-3,4,4 thiazolidine thione-2

: 80102-38-1,93625-10-6
5-imino-3,4,4-trimethyl-thiazolidine-2-thione; compound with 5,5-dimethyl-imidazolidine-2,4-dithione

: 2-Isothiocyanato-2-methyl-thiopropionamide

Guidance literature:: at 50 ℃; Product distribution; Heating; influence of reaction time and acidification on the product distribution; ammonia or methylamine as accelerator of the reaction;