Tests with repellents against the American dog tick was written by Cole, M. M.;Lloyd, Geo. W.. And the article was included in Journal of Economic Entomology in 1955.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol The following contents are mentioned in the article:
Di-Bu adipate (I) repelled 86% of Dermacentor variablis when applied at the rate of 2 g. per sq. ft. of trouser cloth. Percentage repellence of mixts of equal parts of 2-butyl-2-ethyl-1,3-propanediol (II), benzyl benzoate (III), and N-butylacetanilide (IV) was 93%, equal parts of II, III, and IV with 1% lindane 89% equal parts of I, II, and IV 86%, equal parts of N-butyl-4-cyclohexene-1,2-dicarboximide (V), undecenoic acid (VI) and IV 83%, equal parts of II, III, and N-propylacetanilide 76%, equal parts of II, IV, and VI 75%, equal parts of I, II, and III 73%, equal parts of II, IV, and V 72%, and equal parts of II, III, and N-isopropylacetanilide 65%. This study involved multiple reactions and reactants, such as 2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol).
2-Butyl-2-ethylpropane-1,3-diol (cas: 115-84-4) belongs to alcohols. Because alcohols are easily synthesized and easily transformed into other compounds, they serve as important intermediates in organic synthesis. Alcohols may be oxidized to give ketones, aldehydes, and carboxylic acids. These functional groups are useful for further reactions. Oxidation of organic compounds generally increases the number of bonds from carbon to oxygen (or another electronegative element, such as a halogen), and it may decrease the number of bonds to hydrogen.Application In Synthesis of 2-Butyl-2-ethylpropane-1,3-diol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts