65160-14-7 Usage
Uses
Used in Agricultural Applications:
2,3-carbonyldimercapto-[1,4]naphthoquinone is used as an insecticide and acaricide for controlling pests such as mites, lice, and ticks in agricultural settings. It is effective in managing these pests by inhibiting chitin synthesis in their exoskeletons, which is crucial for their growth and development, ultimately leading to their death.
Used in Veterinary Applications:
In the veterinary industry, 2,3-carbonyldimercapto-[1,4]naphthoquinone is used as a treatment for controlling pests on animals. It helps in managing infestations of mites, lice, and ticks, which can cause discomfort and health issues in animals. By disrupting the chitin synthesis and nervous system function in these pests, igr contributes to their elimination and prevention of further infestations.
Environmental Considerations:
2,3-carbonyldimercapto-[1,4]naphthoquinone is considered toxic to aquatic organisms. Therefore, it is essential to use 2,3-carbonyldimercapto-[1,4]naphthoquinone with caution and follow proper guidelines to minimize its environmental impact. This includes avoiding its use near water bodies and ensuring proper disposal of any leftover product to prevent contamination of aquatic ecosystems.
Formulations:
2,3-carbonyldimercapto-[1,4]naphthoquinone is available in various formulations to cater to different application needs. These include dusts, emulsifiable concentrates, and wettable powders, which can be tailored to specific agricultural or veterinary requirements for effective pest control.
Check Digit Verification of cas no
The CAS Registry Mumber 65160-14-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,6 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65160-14:
(7*6)+(6*5)+(5*1)+(4*6)+(3*0)+(2*1)+(1*4)=107
107 % 10 = 7
So 65160-14-7 is a valid CAS Registry Number.
65160-14-7Relevant academic research and scientific papers
Watson,Eduok,Kashyap,Krawiec
, p. 3035 - 3042 (1993)
Benzocyclohexa-2,5-diene-1,4-dione-1,3-thiole-2-thione (2) was synthesized starting with 2,3-dichloronapthoquinone (1). Compounds 3 and 4 were also obtained; however, the yield of 2 can be increased through control of the temperature and reaction time. Reaction of 2 with triethylphosphite gave 5 and the tetrathiafulvalene ester 6. The tetrathiafulvalenequinone (9) was obtained by hydrolysis of 6 followed by oxidation of 8. Compound 9 was obtained more directly by hydrogenation of 2 followed by coupling with triethylphosphite and oxidation. Chloranil was used to prepare the dithiafulvene quinone 12 which was reduced, coupled with triethylphosphite to form, presumably, polymer 13. The reactions were repeated using the hexanoic acid esters of the corresponding hydroquinone thiafulvalenes. The crystal structures of 2, 3, 4, 5, 6a and 10 were determined by X-ray diffraction. Cyclic voltammetry studies show the tetrathiafulvalene quinones reduce like quinones, but do not exhibit the oxidation properties of tetrathiafulvalenes.
