Cyclohexyldithiocarbamic acid triethylamine salt

Base Information

• Chemical Name: Cyclohexyldithiocarbamic acid triethylamine salt
• CAS No.: 43009-21-8
• Molecular Formula: C7H13NS2.C6H15N
• Molecular Weight: 276.511
• DSSTox Substance ID: DTXSID70494255
• Mol file: 43009-21-8.mol

Synonyms:43009-21-8;cyclohexyldithiocarbamic acid triethylamine salt;SCHEMBL11250337;DTXSID70494255;POCAPNGEMGYDKF-UHFFFAOYSA-N;Cyclohexylcarbamodithioic acid--N,N-diethylethanamine (1/1)

Chemical Property of Cyclohexyldithiocarbamic acid triethylamine salt

Chemical Property:

• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 276.16939125
• Heavy Atom Count: 17
• Complexity: 144

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCN(CC)CC.C1CCC(CC1)NC(=S)S

Technology Process of Cyclohexyldithiocarbamic acid triethylamine salt

There total 1 articles about Cyclohexyldithiocarbamic acid triethylamine salt 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: 90.0%

carbon disulfide (75-15-0,12122-00-8) + cyclohexylamine (108-91-8,157973-60-9) + triethylamine (121-44-8) → Cyclohexyl-dithiocarbamic acid; compound with triethyl-amine (43009-21-8)

Guidance literature:

In diethyl ether; at 0 ℃; for 72h;

DOI:10.3184/030823409X12561978806846

Reference yield: 92.0%

Cyclohexyl-dithiocarbamic acid; compound with triethyl-amine (43009-21-8) → isothiocyanatocyclohexane (1122-82-3)

Guidance literature:

With 2-chloro-1,3-dimethylimidazolinium chloride; triethylamine; In dichloromethane; at 20 ℃; for 13h;

DOI:10.1021/jo990210y

Reference yield: 72.0%

1,1,3-tricyano-2-amino-1-propene (868-54-2) + Cyclohexyl-dithiocarbamic acid; compound with triethyl-amine (43009-21-8) → 2-amino-1-cyclohexyl-4-imino-6-mercapto-1,4-dihydropyridine-3,5-dicarbonitrile

Guidance literature:

With triethylamine; In N,N-dimethyl-formamide; at 100 ℃; for 2h;

DOI:10.1080/17415993.2015.1102911

upstream raw materials:

carbon disulfide

cyclohexylamine

triethylamine

Downstream raw materials:

isothiocyanatocyclohexane

1-cyclohexyl-5-mercapto-1H-tetrazole

N-cyclohexylthiourea

2-(cyclohexylimino)naphtho[2,3-d][1,3]dithiole-4,9-dione

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