4707-16-8 Usage
Uses
Used in Laboratory Research:
2,3,5,6-Tetrachlorobenzene-1-thiol is utilized as a building block for the synthesis of various organic compounds, contributing to the development of new chemical entities and materials.
Used in Pesticide Industry:
2,3,5,6-TETRACHLOROBENZENE-1-THIOL serves as a pesticide, helping to control and manage pests in agricultural settings, thereby protecting crops and ensuring food security.
Used as an Intermediate in Chemical Production:
2,3,5,6-Tetrachlorobenzene-1-thiol is employed as an intermediate in the production of dyes and other chemical products, playing a crucial role in the manufacturing process of these substances.
However, it is important to note that due to the toxic and potentially harmful effects of 2,3,5,6-tetrachlorobenzene-1-thiol on human health and the environment, strict safety measures and regulations must be adhered to during its handling and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 4707-16-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4707-16:
(6*4)+(5*7)+(4*0)+(3*7)+(2*1)+(1*6)=88
88 % 10 = 8
So 4707-16-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H2Cl4S/c7-2-1-3(8)5(10)6(11)4(2)9/h1,11H
4707-16-8Relevant academic research and scientific papers
Elemental sulfur as a sulfuration agent in the copper-catalyzed C-H bond thiolation of electron-deficient arenes
Yan, Haiming,Huang, Zhiliang,Chen, Meng,Li, Cuiting,Chen, Ya,Gao, Meng,Lei, Aiwen
supporting information, p. 8276 - 8279 (2017/10/23)
By utilizing elemental sulfur as the thiolation agent and oxidant, a copper-catalyzed direct C-H bond thiolation of electron-deficient arenes was demonstrated. Various electron-deficient arenes were proved to be suitable for this transformation. Preliminary mechanistic studies indicated that this reaction underwent a radical pathway, in which the trisulfur radical anion (S3-) might play a vital role. Meanwhile, KIE experiments suggested that C-H bond cleavage was not involved in the rate-determining step.
Metabolism of 2,3,5,6-tetrachloronitrobenzene (tecnazene) in rat
Lappin,Pritchard,Moore,Laird
, p. 65 - 77 (2007/10/03)
The metabolic fate of [U-14C]-2,3,5,6-tetrachloronitrobenzene (tecnazene) has been determined in the male and female rat following a single dose of 1 mg/kg and in surgically prepared, bile-duct-cannulated rats following a single oral dose of 13
