59819-52-2 Usage
Description
(2-CHLOROPHENYL)(2,2,2-TRICHLOROETHYL) CHLOROPHOSPHATE, commonly known as CHLORPHOS, is an organophosphate compound that functions as an insecticide and acaricide. It operates by inhibiting acetylcholinesterase, a critical enzyme for the nervous system's proper functioning in insects, leading to overstimulation, paralysis, and death of the targeted pests. Due to its high toxicity to both insects and mammals, CHLORPHOS requires careful handling and is classified as a restricted use pesticide by the Environmental Protection Agency to mitigate the risks of acute and chronic toxicity.
Used in Pest Control Industry:
CHLORPHOS is used as an insecticide and acaricide for controlling a variety of pests in agriculture and other settings. Its application is aimed at protecting crops and reducing damage caused by insects, thereby ensuring higher yields and better quality produce. Due to its high potency and effectiveness, it is a preferred choice in situations where pest infestations are severe or resistant to other treatments.
Used in Public Health:
In public health settings, CHLORPHOS is used for controlling disease-transmitting insects such as mosquitoes, ticks, and fleas. Its application helps in reducing the spread of vector-borne diseases, thus contributing to improved public health and well-being.
Used in Veterinary Medicine:
CHLORPHOS is also utilized in veterinary medicine for treating and preventing infestations in livestock and pets. Its application ensures the health and comfort of animals by eliminating parasites that can cause various health issues and discomfort.
Check Digit Verification of cas no
The CAS Registry Mumber 59819-52-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,1 and 9 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59819-52:
(7*5)+(6*9)+(5*8)+(4*1)+(3*9)+(2*5)+(1*2)=172
172 % 10 = 2
So 59819-52-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Cl5O3P/c9-6-3-1-2-4-7(6)16-17(13,14)15-5-8(10,11)12/h1-4H,5H2
59819-52-2Relevant articles and documents
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Boom et al.
, p. 869 (1976)
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Enzymatic process for 3-substituted cephalosporins
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, (2008/06/13)
6β-(3-Carboxyphenylacetylamino)-2α-substituted--2β-methylpenam-3-carboxylic acids and 6β-adipoylamino--2α-substituted-2β-methylpenam-3-carboxylic acids, wherein the α-substituent is C1-C3 alkyl, C1-C3 alkoxy, vinyl or allenyl, are converted by the enzyme deacetoxy-cephalosporin C synthetase to the 7β-(3-carboxyphenyl-acetylamino)-3-substituted-3-cephem-4-carboxylic acid and the 7β-adipoylamino-3-substituted-3-cephem-4-car-boxylic acid.