65160-14-7 Usage
General Description
2,3-carbonyldimercapto-[1,4]naphthoquinone, also known as igr, is an organic compound with the chemical formula C10H6O2S2. It is commonly used as an insecticide and acaricide to control pests such as mites, lice, and ticks in agricultural and veterinary applications. This chemical works by inhibiting the chitin synthesis in the exoskeleton of the target pests, leading to their death. Its mode of action also involves disrupting the normal function of the nervous system in insects. However, igr is considered toxic to aquatic organisms and should be used with caution to minimize environmental impact. It is available in various formulations such as dusts, emulsifiable concentrates, and wettable powders for different applications.
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 articles and documents
Tetrathiafulvalene quinones, hydroquinones and esters
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.
