10059-66-2 Usage
Uses
Used in Pesticide Industry:
5,6,7,8,9,9-hexachloro-1,2,3,4,4a,5,8,8a-octahydro-1,4:5,8-dimethanonaphthalen-2-ol is used as an insecticide for its toxic and environmental persistence properties. It effectively controls pests in agricultural settings, contributing to increased crop yields and protection against infestations.
However, due to its potential for causing harm to humans and the environment, the use and production of 5,6,7,8,9,9-hexachloro-1,2,3,4,4a,5,8,8a-octahydro-1,4:5,8-dimethanonaphthalen-2-ol have been regulated and restricted in many countries. This is to mitigate the risks associated with its long-term exposure and accumulation in ecosystems, as well as to promote the development and adoption of safer and more sustainable alternatives in pest management.
Check Digit Verification of cas no
The CAS Registry Mumber 10059-66-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,0,5 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10059-66:
(7*1)+(6*0)+(5*0)+(4*5)+(3*9)+(2*6)+(1*6)=72
72 % 10 = 2
So 10059-66-2 is a valid CAS Registry Number.
10059-66-2Relevant articles and documents
Study of the kinetic resolution of (±)-10-exo-hydroxy-pentacyclo[6.2.1.13,6.02,7.0 5,9]dodeca-4-one by lipase catalysis and the intramolecular racemization of the pure enantiomer by thermal dyotropic reaction
Martins, Jose E. D.,Alifantes, Joao,Pohlmann, Adriana R.,Costa, Valentim E. U.
, p. 683 - 688 (2007/10/03)
In this work, the modified synthesis of (±)-10-exo-hydroxy-pentacyclo[6.2.1.13,6.02,7.0 5,9]dodeca-4-one (±)-10 as well as its resolution by lipase-catalyzed transesterification with vinyl acetate is described. A thermal racemization process of (+)-10 to (±)-10 was observed. A mechanism involving racemization of (+)-10 through dyotropic intramolecular hydrogen migration is proposed and supported by computational analysis.
