2314-49-0

Basic information

• Product Name: diethyl trithiocarbonate
• Synonyms: diethyl trithiocarbonate;Carbonotrithioic acid=diethyl ester;Trithiocarbonic acid diethyl ester
• CAS NO: 2314-49-0
• Molecular Formula: C₅H₁₀S₃
• Molecular Weight: 166.3279
• EINECS: 219-012-4
• Mol File: 2314-49-0.mol
• Article Data: 18

Chemical Properties

• Boiling Point: 282.1°Cat760mmHg
• Flash Point: 124.4°C
• Appearance: /
• Density: 1.155g/cm³
• Vapor Pressure: 0.00584mmHg at 25°C
• Refractive Index: 1.588
• CAS DataBase Reference: diethyl trithiocarbonate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl trithiocarbonate(2314-49-0)
• EPA Substance Registry System: diethyl trithiocarbonate(2314-49-0)

Safety Data

• Hazardous Substances Data: 2314-49-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C5H10S3/c1-3-7-5(6)8-4-2/h3-4H2,1-2H3

Upstream product

• 56-23-5 tetrachloromethane 
• 6267-24-9 tris(ethylsulfanyl)methane 
• 74-96-4 ethyl bromide 
• 33145-02-7 2,2'-<1,2-ethanediylbis(thio)>bis-1,3-dithiolane 
• 10219-97-3 bis(ethylsulfanylthiocarbonyl) disulfide 
• 857790-16-0 bis-ethylsulfanylthiocarbonyl-trisulfane 
• 117891-12-0 bis-ethylsulfanylthiocarbonyl-tetrasulfane 
• 75-03-6 ethyl iodide 
• 584-10-1 potassium trithiocarbonate 
• 75-15-0 carbon disulfide 
• 105-36-2 ethyl bromoacetate 
• 80-40-0 ethyl ester of p-toluenesulfonic acid 
• 75-08-1 ethanethiol 
• 811-50-7 mercury(II) ethanethiolate 

Downstream Products

• 102081-15-2 4-butyl-1,2-diphenyl-5-thioxo-pyrazolidin-3-one 
• 75-08-1 ethanethiol 
• 1371586-34-3 ethyl 2-methyl-3-oxo-3-phenylpropane(dithioate) 
• 89880-06-8 3,3-bis(ethylthio)-2-methylsulphinyl-1-(p-nitrophenyl)prop-2-enol 
• 1147550-11-5 ammonium thiocyanate 
• 594-45-6 ethanesulfonic acid 
• 37147-15-2 5-ethylsulfanyl-3H-[1,3,4]thiadiazole-2-thione 
• 53723-88-9 (5-thioxo-4,5-dihydro-[1,3,4]thiadiazol-2-ylmercapto)-acetic acid 
• 352-93-2 diethyl sulphide 
• 6267-24-9 tris(ethylsulfanyl)methane 
• 35994-88-8 tetrakis(ethylthio)ethene 
• 4396-19-4 bis(ethylthio)methane 
• 75-15-0 carbon disulfide 

Relevant articles and documents

A facile KF/Al2O3-mediated, one-pot synthesis of symmetrical trithiocarbonates from alkyl halides and carbon disulfide

A facile, efficient, and convenient method has been developed for the one-pot synthesis of symmetrical trithiocarbonates from carbon disulfide and various alkyl halides in the presence of KF/Al2O3 in DMF at room temperature. Copyright

A convenient one-pot method for the synthesis of symmetrical dialkyl trithiocarbonates using NH4OAc under mild neutral conditions

A facial, new, one-pot method for the preparation of symmetrical organic trithiocarbonates from various alkyl halides and carbon disulfide is described. This is a convenient, clean, and mild procedure, which involves the use of the neutral, nontoxic, commercially available, and inexpensive reagent NH4OAc in the preparation of the trithiocarbonate ion from carbon disulfide.

Investigations of the Thermal Responsiveness of 1,4,2-Oxathiazoles

The first systematic study of the thermal rearrangement/fragmentation of 5,5-disubstituted 1,4,2-oxathiazoles into isothiocyanates is reported. Structure-activity relationships reveal that the choice of substituent at the 5-position of the 1,4,2-oxathiazoles is the predominant factor to influence the ease of fragmentation.

K3PO4-mediated one-pot synthesis of symmetrical trithiocarbonates

A new procedure has been developed for synthesis of symmetrical trithiocarbonates by one-pot reaction of carbon disulfide, and various alkyl halides in dimethylformamide using K3PO4 as an inexpensive and effective reagent.