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  2. Glycine methyl ester hydrochloride - Wikipedia

    en.wikipedia.org/wiki/Glycine_methyl_ester...

    Glycine methyl ester hydrochloride is the organic compound with the formula [CH 3 O 2 CCH 2 NH 3]Cl. A white, water-soluble solid, it is the hydrochloride of the methyl ester of the amino acid glycine .

  3. Glycine - Wikipedia

    en.wikipedia.org/wiki/Glycine

    Pyrolysis of glycine or glycylglycine gives 2,5-diketopiperazine, the cyclic diamide. [35] Glycine forms esters with alcohols. They are often isolated as their hydrochloride, such as glycine methyl ester hydrochloride. Otherwise, the free ester tends to convert to diketopiperazine. As a bifunctional molecule, glycine reacts with many reagents.

  4. Ethyl diazoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_diazoacetate

    Ethyl diazoacetate (N=N=CHC(O)OC 2 H 5) is a diazo compound and a reagent in organic chemistry.It was discovered by Theodor Curtius in 1883. [4] The compound can be prepared by reaction of the ethyl ester of glycine with sodium nitrite and sodium acetate in water.

  5. Carbamate - Wikipedia

    en.wikipedia.org/wiki/Carbamate

    IUPAC states "The esters are often called urethanes or urethans, a usage that is strictly correct only for the ethyl esters." [ 44 ] But also states, "An alternative term for the compounds R2NC(=O)OR' (R' not = H), esters of carbamic acids, R,NC(=O)OH, in strict use limited to the ethyl esters, but widely used in the general sense". [ 45 ]

  6. Glycine (data page) - Wikipedia

    en.wikipedia.org/wiki/Glycine_(data_page)

    The complete data for Glycine. General information. Chemical formula: C 2 H 5 N O 2 ...

  7. Sarcosine - Wikipedia

    en.wikipedia.org/wiki/Sarcosine

    Sarcosine is an intermediate in the metabolism of choline to glycine. [2] Sarcosine, like the related compounds dimethylglycine (DMG) and trimethylglycine (betaine, TMG), is formed via the metabolism of nutrients such as choline and methionine, which both contain methyl groups used in a wide range of

  8. Glycylglycine - Wikipedia

    en.wikipedia.org/wiki/Glycylglycine

    Glycylglycine is the dipeptide of glycine, making it the simplest peptide. [1] The compound was first synthesized by Emil Fischer and Ernest Fourneau in 1901 by boiling 2,5-diketopiperazine (glycine anhydride) with hydrochloric acid. [2] Shaking with alkali [1] and other synthesis methods have been reported. [3]

  9. Glycolic acid - Wikipedia

    en.wikipedia.org/wiki/Glycolic_acid

    He proposed that the amino acid glycine—which was then called glycocolle—might be the amine of a hypothetical acid, which he called "glycolic acid" (acide glycolique). [5] Glycolic acid was first prepared in 1851 by German chemist Adolph Strecker (1822–1871) and Russian chemist Nikolai Nikolaevich Sokolov (1826–1877).