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  2. Methyl group - Wikipedia

    en.wikipedia.org/wiki/Methyl_group

    [15] [16] The term "methyl" was derived in about 1840 by back-formation from "methylene", and was then applied to describe "methyl alcohol" (which since 1892 is called "methanol"). Methyl is the IUPAC nomenclature of organic chemistry term for an alkane (or alkyl) molecule, using the prefix "meth-" to indicate the presence of a single carbon.

  3. Methanol - Wikipedia

    en.wikipedia.org/wiki/Methanol

    The term "methyl" was derived in about 1840 by back-formation from "methylene", and was then applied to describe "methyl alcohol". This was shortened to "methanol" in 1892 by the International Conference on Chemical Nomenclature. [29] The suffix-yl, which, in organic chemistry, forms names of carbon groups, is from the word methyl.

  4. Methylation - Wikipedia

    en.wikipedia.org/wiki/Methylation

    Methylation, in the chemical sciences, is the addition of a methyl group on a substrate, or the substitution of an atom (or group) by a methyl group. Methylation is a form of alkylation, with a methyl group replacing a hydrogen atom. These terms are commonly used in chemistry, biochemistry, soil science, and biology.

  5. Alkyl group - Wikipedia

    en.wikipedia.org/wiki/Alkyl_group

    In organic chemistry, an alkyl group is an alkane missing one hydrogen. [1] The term alkyl is intentionally unspecific to include many possible substitutions. An acyclic alkyl has the general formula of −C n H 2n+1. A cycloalkyl group is derived from a cycloalkane by removal of a hydrogen atom from a ring and has the general formula −C n H ...

  6. Methylene group - Wikipedia

    en.wikipedia.org/wiki/Methylene_group

    Acidity of diethyl malonate, a 1,3-dicarbonyl compound. The central carbon in 1,3-dicarbonyl compound is known as an activated methylene group. This is because, owing to the structure, the carbon is especially acidic and can easily be deprotonated to form a methylene group. [4]

  7. Methyl radical - Wikipedia

    en.wikipedia.org/wiki/Methyl_radical

    The carbon centre in methyl can bond with electron-donating molecules by reacting: CH • 3 + R • → RCH 3. Because of the capture of the nucleophile (R •), methyl has oxidising character. Methyl is a strong oxidant with organic chemicals. However, it is equally a strong reductant with chemicals such as water.

  8. Hydroxymethyl group - Wikipedia

    en.wikipedia.org/wiki/Hydroxymethyl_group

    The hydroxymethyl group is a substituent with the structural formula −CH 2 −OH.It consists of a methylene bridge (−CH 2 − unit) bonded to a hydroxyl group (−OH).This makes the hydroxymethyl group an alcohol.

  9. 3-Methoxytyramine - Wikipedia

    en.wikipedia.org/wiki/3-Methoxytyramine

    3-Methoxytyramine (3-MT), also known as 3-methoxy-4-hydroxyphenethylamine, is a human trace amine and the major metabolite of the monoamine neurotransmitter dopamine. [1] [2] It is formed by the introduction of a methyl group to dopamine by the enzyme catechol-O-methyltransferase (COMT). 3-MT can be further metabolized by the enzyme monoamine oxidase (MAO) to form homovanillic acid (HVA ...