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  2. 2-Ethylphenol - Wikipedia

    en.wikipedia.org/wiki/2-Ethylphenol

    2-Ethylphenol is an organic compound with the formula C 2 H 5 C 6 H 4 OH. It is one of three isomeric ethylphenols. A colorless liquid, it occurs as an impurity in xylenols and as such is used in the production of commercial phenolic resins. It is produced by ethylation of phenol using ethylene or ethanol in the presence of aluminium phenolate. [2]

  3. Phenols - Wikipedia

    en.wikipedia.org/wiki/Phenols

    Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide: [citation needed] CH 2 =CR 2 + C 6 H 5 OH → R 2 CHCH 2 -2-C 6 H 4 OH More than 100,000 tons of tert-butyl phenols are produced annually (year: 2000) in this way, using isobutylene (CH 2 =CMe 2 ) as the alkylating agent.

  4. Acid dissociation constant - Wikipedia

    en.wikipedia.org/wiki/Acid_dissociation_constant

    Pauling's second rule is that the value of the first pK a for acids of the formula XO m (OH) n depends primarily on the number of oxo groups m, and is approximately independent of the number of hydroxy groups n, and also of the central atom X. Approximate values of pK a are 8 for m = 0, 2 for m = 1, −3 for m = 2 and < −10 for m = 3. [28]

  5. 2,6-Di-tert-butylphenol - Wikipedia

    en.wikipedia.org/wiki/2,6-Di-tert-butylphenol

    Of particular note is methyl-3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate (CAS# 6386-38-5), which is formed by the Michael addition of methyl acrylate. This compound is used as a feedstock in the synthesis of more complex antioxidants such as Irganox 1098 . 2,6-Di- tert -butylphenol is also used in the synthesis of CGP-7930 , probucol , and ...

  6. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    Anisole (C 6 H 5 OCH 3) is the simplest phenol ether, and is a versatile precursor for perfumes and pharmaceuticals. [1] Vanillin and ethylvanillin are phenol ether derivatives commonly utilized in vanilla flavorings and fragrances, while diphenyl ether is commonly used as a synthetic geranium fragrance.

  7. Alkylphenol - Wikipedia

    en.wikipedia.org/wiki/Alkylphenol

    Alkylphenols are xenoestrogens. [3] Long chain Alkylphenols have the most potent estrogenic activity. [3] The European Union has implemented sales and use restrictions on certain applications in which nonylphenols are used because of their alleged "toxicity, persistence, and the liability to bioaccumulate" but the United States EPA has taken a slower approach to make sure that action is based ...

  8. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents.

  9. Acid strength - Wikipedia

    en.wikipedia.org/wiki/Acid_strength

    Any acid with a value which is less than about -2 behaves as a strong acid. This results from the very high buffer capacity of solutions with a pH value of 1 or less and is known as the leveling effect. [3] The following are strong acids in aqueous and dimethyl sulfoxide solution.