102996-33-8 Usage
Uses
Used in Agricultural Applications:
5-Chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carbonitrile is used as a pesticide in agriculture for controlling pests such as insects and fungi. It operates by disrupting the nervous system of the target organisms, which results in their death, thereby protecting crops from damage.
Used in Public Health Applications:
In the realm of public health, 5-Chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carbonitrile is used to control disease vectors like mosquitoes. Its application helps in reducing the spread of diseases transmitted by these vectors, contributing to improved public health outcomes.
Used in Pharmaceutical Research:
5-Chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carbonitrile is also being explored for its potential pharmaceutical applications, particularly in the development of new fungicides. Its chemical properties are of interest to researchers looking to innovate in the field of antifungal treatments.
It is crucial to handle 5-Chloro-1-(3-chlorophenyl)-1H-pyrazole-4-carbonitrile with care due to its toxic nature. Proper use and safety measures are essential to prevent harm to humans and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 102996-33-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,9,9 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 102996-33:
(8*1)+(7*0)+(6*2)+(5*9)+(4*9)+(3*6)+(2*3)+(1*3)=128
128 % 10 = 8
So 102996-33-8 is a valid CAS Registry Number.
102996-33-8Relevant academic research and scientific papers
Herbicidal 5-halo-1-halophenyl-1H-pyrazole-4-carbonitriles
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, (2008/06/13)
The present invention is directed to herbicidal compounds of the formula STR1 wherein each R1 independently is halogen; R2 is halo or trifluoromethyl; and n is 1-5; with the provisos that when n is 1, R1 is other than fluorine, and when n is 2 and each R1 is chlorine, at least one R1 is located at a para or ortho position on the phenyl ring.
