Ethanedithioamide, N,N-dimethyl-

Base Information

• Chemical Name: Ethanedithioamide, N,N-dimethyl-
• CAS No.: 41168-91-6
• Molecular Formula: C4H8N2S2
• DSSTox Substance ID: DTXSID90388248
• Nikkaji Number: J1.080.255E
• Mol file: 41168-91-6.mol

Synonyms:Ethanedithioamide, N,N-dimethyl-;N',N'-dimethylethanedithioamide;41168-91-6;N,N-Dimethyldithioxamide;N,N-dimethyl-dithio-oxamide;SCHEMBL6683290;DTXSID90388248;AKOS006340982

Chemical Property of Ethanedithioamide, N,N-dimethyl-

Chemical Property:

• XLogP3: 0.2
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 148.01289061
• Heavy Atom Count: 8
• Complexity: 119

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C)C(=S)C(=S)N

Technology Process of Ethanedithioamide, N,N-dimethyl-

There total 2 articles about Ethanedithioamide, N,N-dimethyl- 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: 25.0%

N,N-Dimethyl-2-nitroacetamid (78920-92-0) → N,N-Dimethyldithiooxamid (41168-91-6) + N,N-Dimethylcyanthioformamid (16703-47-2)

Guidance literature:

With Lawessons reagent; In toluene; at 100 ℃; for 0.25h; other reagent;

DOI:10.1016/S0040-4039(00)99198-6

Reference yield: 16.0%

N,N-Dimethyl-2-nitroacetamid (78920-92-0) → NO,NO-dimethylmonothiooxamide (18138-14-2) + N,N-Dimethyldithiooxamid (41168-91-6) + C5H10N2O2S

Guidance literature:

With Lawessons reagent; In toluene; at 80 ℃; for 0.5h; Heating; 2.) warm methanol, 15 min;

DOI:10.1016/S0040-4039(00)99198-6

Reference yield:

N,N-Dimethyldithiooxamid (41168-91-6) + 4-Nitrophenacyl bromide (99-81-0) → 4-(4-nitro-phenyl)-thiazole-2-carbothioic acid dimethylamide (69792-57-0)

Guidance literature:

In ethanol;

upstream raw materials:

N,N-Dimethyl-2-nitroacetamid

Downstream raw materials:

4-(4-nitro-phenyl)-thiazole-2-carbothioic acid dimethylamide

4-(4-bromo-phenyl)-thiazole-2-carbothioic acid dimethylamide

4-(4-propoxy-phenyl)-thiazole-2-carbothioic acid dimethylamide

4-(4-methoxy-phenyl)-thiazole-2-carbothioic acid dimethylamide

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