71906-18-8 Usage
Organochlorine class
Member of a class of chemicals containing carbon and chlorine This classification means the compound has potential environmental persistence and bioaccumulation due to its chemical structure.
Primary use
Pesticide and fungicide The main applications of 2-(1,2,4,5-Tetrachlorophenyl)-3,4,5-trichlorothiophene are to control pests and fungi in agricultural and horticultural settings.
Insecticidal properties
Strong The compound is highly effective in controlling and killing insects.
Acaricidal properties
Strong The compound is also highly effective in controlling and killing mites and ticks (acari).
Range of pests and parasites
Wide The compound is effective against a broad spectrum of pests and parasites, making it useful in various agricultural and horticultural applications.
Toxicity to non-target organisms
Highly toxic The compound can cause harm to humans and other non-target organisms, posing potential environmental and health risks.
Regulatory restrictions
Many countries Due to its potential risks, the compound has faced regulatory restrictions in numerous countries.
Use limitations
Increasingly limited in favor of safer alternatives As a result of its toxicity and environmental concerns, the compound's use is declining in favor of safer and more environmentally friendly options.
Check Digit Verification of cas no
The CAS Registry Mumber 71906-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,0 and 6 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 71906-18:
(7*7)+(6*1)+(5*9)+(4*0)+(3*6)+(2*1)+(1*8)=128
128 % 10 = 8
So 71906-18-8 is a valid CAS Registry Number.
71906-18-8Relevant academic research and scientific papers
Rahman, Mohammed T.
, p. 91 - 94 (1982)
Two novel polychlorinated unsymmetrical biaryls viz., 2-(1,2,4,5-tetrachlorophenyl)-3,4,5-trichlorothiophene and 2-(1,2,4,5-tetrachlorophenyl)-3,4-dichlorothiophene have been prepared in 56 - 58 percent yields by reacting 1,2,4,5-tetrachloro-3-iodobenzene
