1085-62-7 Usage
Description
(1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-en-2-yl)methyl acetate is a synthetic chemical compound with a complex molecular structure. It is a derivative of the naturally occurring compound, bicyclic monoterpenoid, and belongs to the class of chlorinated compounds. This chemical has been developed for use in insecticides and pesticides due to its strong insecticidal properties.
Used in Pesticide Industry:
(1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-en-2-yl)methyl acetate is used as an insecticide for its strong insecticidal properties. It is effective in controlling various pests that can damage crops and other plants.
However, it is important to note that (1,4,5,6,7,7-hexachlorobicyclo[2.2.1]hept-5-en-2-yl)methyl acetate is also known to be highly toxic to humans and the environment. Its use is regulated and restricted in many countries due to its potential risks. The chemical is considered a persistent organic pollutant because of its long-term persistence in the environment and its potential to bioaccumulate in the food chain. As a result, there is ongoing research and regulatory efforts to assess and minimize the risks associated with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 1085-62-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,8 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1085-62:
(6*1)+(5*0)+(4*8)+(3*5)+(2*6)+(1*2)=67
67 % 10 = 7
So 1085-62-7 is a valid CAS Registry Number.
1085-62-7Relevant articles and documents
Enzymatic resolution of (±)-2-endo-hydroxymethyl and acetoxymethyl substituted hexachloronorbornene derivatives
Tuerkmen, Yunus Emre,Akhmedov, Idris Mecidoglu,Tanyeli, Cihangir
, p. 2315 - 2318 (2007/10/03)
(±)-2-endo-Hydroxymethyl-1,4,5,6,7,7-hexachlorobicyclo[2.2.1] hept-5-ene and (±)-2-endo-acetoxymethyl-1,4,5,6,7,7-hexachlorobicyclo[2. 2.1]hept-5-ene were resolved by using various hydrolases to afford enantiomerically enriched products with ees of 94-98%. The absolute configuration was determined by transforming 2-endo-acetoxymethyl-1,4,5,6,7,7- hexachlorobicyclo[2.2.1]hept-5-ene into 2-endo-hydroxymethyl-bicyclo[2.2.1]hept- 5-ene with known absolute configuration.
DIENOPHILIC ACTIVITY OF ALLYL HALOGENOACETATES IN REACTION WITH HEXACHLOROCYCLOPENTADIENE
Guseinov, M. M.,Kyazimova, T. G.,Kurbanova, R. A.,Babaev, R. S.,Shukyurova, M. B.
, p. 1985 - 1988 (2007/10/02)
The kinetics of the diene condensation of hexachlorocyclopentadiene with allyl monochloroacetate, monobromoacetate, and acetate were investigated by GLC.The kinetic and thermodynamic parameters of the reactions were determined.By a comparative analysis of the results it was shown that the nature of the electronwithdrawing substituent affects the dienophilic activity of the allyl esters in diene condensation with hexachlorocyclopentadiene.