2-[(4-Methylphenyl)thio]ethanethioamide

Base Information

Chemical Name:2-[(4-Methylphenyl)thio]ethanethioamide
CAS No.:59865-83-7
Molecular Formula:C₉H₁₁NS₂
Molecular Weight:197.325
Hs Code.:
DSSTox Substance ID:DTXSID301278300

Synonyms:2-[(4-Methylphenyl)thio]ethanethioamide;DTXSID301278300;AKOS014776200;59865-83-7

Suppliers and Price of 2-[(4-Methylphenyl)thio]ethanethioamide

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 2-[(4-Methylphenyl)thio]ethanethioamide

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:197.03329170
Heavy Atom Count:12
Complexity:151

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)SCC(=S)N

Technology Process of 2-[(4-Methylphenyl)thio]ethanethioamide

There total 2 articles about 2-[(4-Methylphenyl)thio]ethanethioamide 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:

: 73623-29-7
2-(4-methylphenylsulfanyl)acetamide

: 59865-83-7
2-p-tolylsulfanyl-thioacetamide

Guidance literature:: With Lawessons reagent; In tetrahydrofuran; at 80 ℃; for 12h;
DOI:10.1016/j.bmcl.2021.127846

Reference yield:

: 3996-29-0
2-[(4-methylphenyl)thio]acetic acid

: 59865-83-7
2-p-tolylsulfanyl-thioacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl dichloride; N,N-dimethyl-formamide / dichloromethane / 2 h / 20 °C

2: ammonia / tetrahydrofuran / 12 h / 20 °C

3: Lawessons reagent / tetrahydrofuran / 12 h / 80 °C

With Lawessons reagent; oxalyl dichloride; ammonia; N,N-dimethyl-formamide; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.bmcl.2021.127846