122-36-1

Basic information

• Product Name: N,N'-DICYCLOHEXYLDITHIOOXAMIDE
• Synonyms: n,n’-dicyclohexyl-ethanedithioamid;LABOTEST-BB LT00159519;N,N'-DICYCLOHEXYLDITHIOOXAMIDE;N,N'-Dicyclohexyldithioxamide;N,N'-Dicyclohexylethanebisthioamide;Ai3-50065;Einecs 204-537-3;Ethanedithioamide, N,N'-dicyclohexyl-
• CAS NO: 122-36-1
• Molecular Formula: C₁₄H₂₄N₂S₂
• Molecular Weight: 284.48
• EINECS: 204-537-3
• Mol File: 122-36-1.mol
• Article Data: 5

Chemical Properties

• Melting Point: 150-154 °C(lit.)
• Boiling Point: 394.2°Cat760mmHg
• Flash Point: 192.2°C
• Appearance: /
• Density: 1.14g/cm³
• PKA: 10.25±0.20(Predicted)
• CAS DataBase Reference: N,N'-DICYCLOHEXYLDITHIOOXAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: N,N'-DICYCLOHEXYLDITHIOOXAMIDE(122-36-1)
• EPA Substance Registry System: N,N'-DICYCLOHEXYLDITHIOOXAMIDE(122-36-1)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36
• WGK Germany: 3
• Hazardous Substances Data: 122-36-1(Hazardous Substances Data)

Usage

General Description

N,N'-DICYCLOHEXYLDITHIOOXAMIDE is a chemical compound with the molecular formula C14H24N2S4. It is commonly used as a chelating agent in the extraction and separation of metal ions. N,N'-DICYCLOHEXYLDITHIOOXAMIDE has a cyclic structure, with two cyclohexyl groups attached to the dithioxoamide functional group. N,N'-DICYCLOHEXYLDITHIOOXAMIDE is known for its ability to form stable complexes with various metal ions, such as copper, nickel, and cobalt, making it useful in processes like hydrometallurgy and environment remediation. It is also used in analytical chemistry and organic synthesis, demonstrating its versatility and importance in various chemical applications.

Upstream product

• 127-18-4 1,1,2,2-tetrachloroethylene 
• 108-91-8 cyclohexylamine 
• 123-91-1 1,4-dioxane 
• 111-34-2 -butyl vinyl ether 
• 33498-03-2 sodium carbonocyanidodithioate 
• 17008-22-9 methyl cyanodithioformate 
• 79-34-5 1,1,2,2-tetrachloroethane 
• 79-01-6 Trichloroethylene 
• 79-40-3 dithiooxamide 
• 131543-46-9 Glyoxal 
• 107-14-2 chloroacetonitrile 
• 74-86-2 acetylene 

Downstream Products

• 162410-88-0 [Hg(N,N'-dicyclohexyldithiooxamide)(SCN)2] 
• 46978-54-5 (N,N'-dicyclohexyldithiooxamidato)copper(II) 
• 93365-95-8 [SnCl₄(C₆H₁₁NHC(S)C(S)NHC₆H₁₁)] 
• 93976-50-2 tetracarbonyl(N,N'-dicyclohexyldithiooxamide)molybdenum 
• 93976-38-6 tricarbonyl(N,N'-dicyclohexyldithiooxamide)(triphenylphosphine)molybdenum 
• 13963-60-5 tris(N,N-diethyldithiocarbamato)cobalt(III) 
• 3299-64-7 N,N'-dicyclohexyloxamide 

Relevant articles and documents

Synthesis of N,N'-Disubstituted Dithiooxamide Derivatives by the Modified Willgerodt–Kindler Reaction

Abstract: The conditions of the reaction of trichloroethylene with sulfur and amines were optimized (the modified Willgerodt–Kindler reaction). The reaction of tetrachloroethylene with sulfur and some basic primary and secondary amines of the aliphatic series in DMF under mild conditions leads to N,N'-disubstituted dithiooxamides in 30–70% yields and with a 100% conversion of tetrachloroethylene.

REACTIVITY OF CYANODITHIOFORMATE TOWARDS PRIMARY AMINES

The two electrophilic carbon atoms of methyl cyanodithioformate 1 are able to react with primary amines giving a variety of different products depending upon the nature of amines.The one step reaction with o-dinucleophiles giving condensed heterocompounds in moderate to good yields is of interest.

STUDIES OF DIOXAMIDE AND DITHIO-OXAMIDE METAL COMPLEXES. PART 2. SYNTHESIS AND SPECTRAL CHARACTERISATION OF RNHC(S)C(S)NHR (R = ALKYL OR ARYL) COMPLEXES WITH SbX3 (X = Cl OR Br), BiCl3, SnX4 (X = Cl OR Br), AND TiCl4. CRYSTAL AND MOLECULAR STRUCTURES OF NN'-DI-ISOPROPYLDITHIO-OXAMIDE ...

The synthesis and characterisation of a variety of SbX3L1.5 (X = Cl or Br), BiCl3L2, SnX4L (X = Cl or Br), and TiCl4L complexes i, Bun, cyclo-C6H11, or CH2Ph> is described.In all cases metal-sulphur bonds are formed following SS'-bidentate ligand attachment.The potential N-donor sites are not involved in co-ordination.The structural characterisation of the uncomplexed ligand PriNHC(S)C(S)NHPri (L3) and the antimony(III) complex SbCl3(L3)1.5 (1) are reported.Crystals of (1) are rhombohedral, space group with a = 11.80(1) Angstroem, α = 60.1(1) deg, and Z = 2. 1089 Unique data above background were collected and the structure refinded to R 0.068.Crystals of L3 are monoclinic, space group P21/c with a = 6.226(7), b = 8.067(11), c = 11.187(12) Angstroem, β = 91.0(1) deg, and Z = 2. 635 Data above background were measured and the structure refinded to R 0.077.The structure of (1) is a three-dimensional polymer.The octahedrally co-ordinated Sb atom lies on a three-fold axis and is strongly bound to three chlorine atoms and also weakly bound to three sulphur atoms from different ligands, which approach their positions trans to chlorine thus giving rise to an octahedral environment.There is no evidence for a stereochemically active lone pair associated with SbIII.In the structure of L3 the sulphur atoms are mutually trans and this orientation is retained on complexation.