10059-98-0 Usage
Uses
Used in Pesticide Production:
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 active ingredient in the production of pesticides and insecticides. Its chemical properties make it effective in controlling pests and insects, contributing to increased crop yields and protection against disease vectors.
Used in Insecticide Production:
In the insecticide 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 a key component for developing insecticidal products. Its potent insecticidal properties help in managing insect populations, reducing the spread of insect-borne diseases, and protecting agricultural produce.
However, due to the potential health and environmental hazards associated with 5,6,7,8,9,9-hexachloro-1,2,3,4,4a,5,8,8a-octahydro-1,4:5,8-dimethanonaphthalen-2-ol, its use is tightly regulated in many countries. Strict safety measures and guidelines are implemented to minimize its impact on the environment and human health.
Check Digit Verification of cas no
The CAS Registry Mumber 10059-98-0 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, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10059-98:
(7*1)+(6*0)+(5*0)+(4*5)+(3*9)+(2*9)+(1*8)=80
80 % 10 = 0
So 10059-98-0 is a valid CAS Registry Number.
10059-98-0Relevant academic research and scientific papers
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.
