856171-16-9 Usage
Uses
Used in Pesticide and Fungicide Applications:
2-Chloro-6-(1-methylethyl)benzothiazole is used as a pesticide and fungicide due to its ability to control and prevent the growth of pests and fungi in various agricultural and horticultural settings. Its chemical properties make it effective in protecting crops and plants from damage caused by these organisms.
Used in Rubber Industry:
In the rubber industry, 2-Chloro-6-(1-methylethyl)benzothiazole is used as an accelerator for the vulcanization of rubber. It enhances the process of cross-linking rubber molecules, resulting in improved strength, elasticity, and durability of the final rubber product.
Precautions:
Due to the potential environmental and health hazards associated with 2-Chloro-6-(1-methylethyl)benzothiazole, its use and handling should be done with proper precautions. This includes adhering to safety regulations, using appropriate protective equipment, and ensuring proper disposal methods to minimize exposure and environmental impact.
Check Digit Verification of cas no
The CAS Registry Mumber 856171-16-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,1,7 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 856171-16:
(8*8)+(7*5)+(6*6)+(5*1)+(4*7)+(3*1)+(2*1)+(1*6)=179
179 % 10 = 9
So 856171-16-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClNS/c1-6(2)7-3-4-8-9(5-7)13-10(11)12-8/h3-6H,1-2H3
856171-16-9Relevant academic research and scientific papers
NOVEL PIPERAZINES, PHARMACEUTICAL COMPOSITIONS AND METHODS OF USE THEREOF
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Page/Page column 90, (2008/06/13)
Disclosed are novel piperazine derivatives that act as agonists of the α7 nAChR. Also disclosed are phannaceutical compositions, methods of treating inflammatory conditions, methods of treating CNS disorders, methods for inhibiting cytokine release from mammalian cells and methods for the preparation of the novel compounds.
A convenient synthesis of 2-mercapto and 2-chlorobenzothiazoles
Zhu, Lei,Zhang, Mingbao,Dai, Miao
, p. 727 - 730 (2007/10/03)
A convenient synthesis of 2-mercapto and 2-chlorobenzothiazoles is described. The key feature of the synthesis is an exclusive ortho-selective nucleophilic aromatic substitution reaction of ortho-haloanilines with potassium/sodium O-ethyl dithiocarbonate under mild conditions. Subsequent intra-molecular cyclization affords 2-mercaptobenzothiazoles in high yields. The 2-mercaptobenzothiazoles are readily converted to corresponding 2-chlorobenzothiazoles upon treatment with sulfuryl chloride.
