16906-70-0

Basic information

• Product Name: Carbamodithioic acid, dimethyl-, phenyl ester
• CAS NO: 16906-70-0
• Molecular Formula: C9H11NS2
• Molecular Weight: 197.325
• Mol File: 16906-70-0.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Carbamodithioic acid, dimethyl-, phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbamodithioic acid, dimethyl-, phenyl ester(16906-70-0)
• EPA Substance Registry System: Carbamodithioic acid, dimethyl-, phenyl ester(16906-70-0)

Safety Data

• Hazardous Substances Data: 16906-70-0(Hazardous Substances Data)

Upstream product

• 71-43-2 benzene 
• 128-04-1 sodium dimethyldithiocarbamate 
• 137-26-8 Thiram 
• 28557-00-8 phenylzinc chloride 
• 79-45-8 N,N-dimethyldithiocarbamic acid 
• 369-57-3 benzenediazonium tetrafluoroborate 
• 66003-76-7 Diphenyliodonium triflate 
• 1483-72-3 diphenyliodonium chloride 
• 722-56-5 diphenyliodonium nitrate 
• 144930-50-7 mesityl(phenyl)iodonium triflouromethanesulfonate 
• 312727-69-8 phenyl(2,4,6-triisopropylphenyl)iodonium trifluoromethanesulfonate 
• 75-15-0 carbon disulfide 
• 88284-48-4 2-(trimethylsilyl)phenyl trifluoromethanesulfonate 
• 124-40-3 dimethyl amine 

Downstream Products

• 139-66-2 diphenyl sulfide 
• 13865-48-0 3-methylphenyl phenyl sulfide 
• 13963-35-4 2-(phenylthio)toluene 
• 5633-55-6 4-phenylsulfanylphenol 
• 55214-86-3 2-phenylsulfanyl-phenol 
• 13343-26-5 phenyl p-chlorophenyl sulfide 
• 65662-88-6 phenyl(4-bromophenyl)sulfide 
• 3699-01-2 4-tolyl phenyl sulfide 
• 54088-93-6 2,6-dimethylphenyl phenyl sulfide 
• 10129-07-4 4-(phenylsulfanyl)benzoic acid ethyl ester 
• 952-97-6 4-nitrophenyl phenyl sulfide 
• 37984-02-4 3-nitrophenyl phenyl sulfide 
• 330-85-8 1-fluoro-4-(phenylthio)benzene 
• 5633-57-8 1-methoxy-4-(phenylsulfanyl)benzene 

Relevant articles and documents

Copper(II)-Promoted Cascade Synthesis of 2-Aminobenzothiazoles Starting from 2-Iodoanilines and Sodium Dithiocarbamates

A facile and efficient formation of 2-aminobenzothiazoles by a copper(II)-promoted one-pot cascade process was developed. The desired 2-aminobenzothiazoles were synthesized in good to excellent yields (up to 97 %) in the presence of Cu(OAc)2 an

Synthesis of Aryl Dithiocarbamates from Tetramethylthiuram Monosulfide (TMTM) and Aryl Boronic Acids: Copper-Catalyzed Construction of C(sp2)-S Bonds

A highly efficient method for the synthesis of S-aryl dithiocarbamates is reported. By using tetramethylthiuram monosulfide (TMTM) and aryl boronic acids as starting materials, C(sp2)-S bondforming reactions proceed smoothly to give the desired aryl dithiocarbamates in good to excellent yields. The methodology features a simple procedure, broad functional group tolerance and excellent yields, whilst showing potential synthetic value for the preparation of a diverse range of biologically and pharmaceutically active compounds.

Aryldithiocarbamates as thiol alternatives in Cu-catalyzed C(aryl)-S coupling reactions using aryldiazonium tetrafluoroborate salts

An efficient method for the synthesis of unsymmetrical diaryl sulfides has been developed by the C-S cross coupling of aryldithiocarbamates and aryldiazonium salts in the presence of CuI-2,2′-bipyridine and Zn. Aryldithiocarbamate compounds have been used here as thiol substitutes. The protocol shows wide substrate scope and good yields of the products.

Copper-Catalyzed Synthesis of S-Aryl Dithiocarbamates from Tetraalkylthiuram Disulfides and Aryl Iodides in Water

An efficient approach for the copper-catalyzed synthesis of aryl dithiocarbamates from aryl iodides and tetraalkylthiuram disulfides in water is described. Without additional ligand and organic solvent, the coupling reaction could provide a series of S-aryl dithiocarbamates in moderate to good yields.