16158-74-0

Basic information

• Product Name: Benzenethiol, 2,4,6-trinitro-, potassium salt
• CAS NO: 16158-74-0
• Molecular Formula: C6H3N3O6S.K
• Molecular Weight: 283.263
• Mol File: 16158-74-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzenethiol, 2,4,6-trinitro-, potassium salt(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenethiol, 2,4,6-trinitro-, potassium salt(16158-74-0)
• EPA Substance Registry System: Benzenethiol, 2,4,6-trinitro-, potassium salt(16158-74-0)

Safety Data

• Hazardous Substances Data: 16158-74-0(Hazardous Substances Data)

Upstream product

• 88-88-0 2,4,6-trinitrochlorobenzene 

Downstream Products

• 2217-06-3 dipicryl sulfide 
• 19404-11-6 methyl-picryl sulfide 
• 37460-71-2 S-2,4,6-Trinitrophenyl-acrylsaeurethioester 
• 37460-65-4 2,4,6-trinitrophenyl ester of methanecarbothioic acid 
• 37460-69-8 S-2,4,6-Trinitrophenyl-γ,γ-dinitrovaleriansaeurethioester 
• 37460-66-5 S-2,4,6-Trinitrophenylpropionsaeurethioester 
• 37460-68-7 S-2,4,6-Trinitrophenyl-α-methyl-γ,γ,γ-trinitrobuttersaeurethioester 
• 37460-67-6 2,4,6-trinitrophenyl ester of χ,χ,χ-trinitropropanecarbothioic acid 
• 37460-72-3 4,4-Dinitro-heptane-bis-thioic acid bis-S-(2,4,6-trinitro-phenyl) ester 
• 37590-58-2 S,S'-bis(2,4,6-trinitrophenyl) dithiooxalate 
• 18738-31-3 3-Amino-2,4,6,2',4',6'-hexanitro-diphenylsulfid 

Relevant articles and documents

INVESTIGATIONS IN THE 2,4,6-TRINITROTHIOPHENOL SERIES. XIV. KINETICS OF THE REACTION OF 3-SUBSTITUTED 2,4,6-TRINITROCHLOROBENZENES WITH POTASSIUM SULFIDE IN DIMETHYLFORMAMIDE

The kinetics of the reaction of 3-R-2,4,6-trinitrochlorobenzenes with potassium sulfide in DMFA were studied by the method of the thermal maximum.The meta substituents can be arranged in the following order according to the degree of activation of the reaction: Cl > OCH3 > H > CH3 > NH2 > O-.A satisfactory correlation was obtained between the logarithms of the rate constants and the Hammett ?m constants.The existence of two-parameter correlations of log k with ?I0 and ?R0 and also with ?I and ?R+, which take account of the contribution from the resonance component to the overall effect of the meta substituent, was established.The good correlation on the ?R0 scale makes it possible to assign the investigated reactions to processes in which there is no direct polar conjugation between the reaction center and the substituent R.