enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Ethyl formate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_formate

    Ethyl formate is an ester formed when ethanol (an alcohol) reacts with formic acid (a carboxylic acid). Ethyl formate has the characteristic smell of rum and is partially responsible for the flavor of raspberries , [ 3 ] occurring naturally in some plant oils, fruits, and juices.

  3. Formate - Wikipedia

    en.wikipedia.org/wiki/Formate

    Formate is a common C-1 source in living systems. It is formed from many precursors including choline, serine, and sarcosine. It provides a C-1 source in the biosynthesis of some nucleic acids. Formate (or formic acid) is invoked as a leaving group in the demethylation of some sterols. [2] These conversions are catalyzed by aromatase enzymes ...

  4. Triethyl orthoformate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_orthoformate

    Triethyl orthoformate (TEOF) is an excellent reagent for converting compatible carboxylic acids to ethyl esters. Such carboxylic acids, refluxed neat in excess TEOF until low-boilers cease evolution, are quantitatively converted to the ethyl esters, without need for extraneous catalysis. [5]

  5. Methyl formate - Wikipedia

    en.wikipedia.org/wiki/Methyl_formate

    Methyl formate, also called methyl methanoate, is the methyl ester of formic acid. The simplest example of a carboxylate ester, it is a colorless liquid with an ethereal odour, high vapor pressure, and low surface tension. It is a precursor to many other compounds of commercial interest. [4]

  6. Ortho ester - Wikipedia

    en.wikipedia.org/wiki/Ortho_ester

    The general formula of orthoesters. In organic chemistry, an ortho ester is a functional group containing three alkoxy groups attached to one carbon atom, i.e. with the general formula RC (OR′)3. Orthoesters may be considered as products of exhaustive alkylation of unstable orthocarboxylic acids and it is from these that the name 'ortho ester ...

  7. Chloroformate - Wikipedia

    en.wikipedia.org/wiki/Chloroformate

    Chloroformate. Chloroformates are a class of organic compounds with the formula ROC (O)Cl. They are formally esters of chloroformic acid. Most are colorless, volatile liquids that degrade in moist air. A simple example is methyl chloroformate, which is commercially available. Chloroformates are used as reagents in organic chemistry. For example ...

  8. Ethyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_chloroformate

    Ethyl chloroformate is an organic compound with the chemical formula ClCO2CH2CH3. It is the ethyl ester of chloroformic acid. It is a colorless, corrosive and highly toxic liquid. It is a reagent used in organic synthesis for the introduction of the ethyl carbamate protecting group [ 3 ] and for the formation of carboxylic anhydrides.

  9. Methyl chloroformate - Wikipedia

    en.wikipedia.org/wiki/Methyl_chloroformate

    Methyl chloroformate is a chemical compound with the chemical formula Cl−C (=O)−O−CH3. It is the methyl ester of chloroformic acid. It is an oily colorless liquid, although aged samples appear yellow. It is also known for its pungent odor.