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  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. Azeotrope tables - Wikipedia

    en.wikipedia.org/wiki/Azeotrope_tables

    Azeotrope tables. This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture ...

  5. 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 ]

  6. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Acetaldehyde (IUPAC systematic name ethanal) is an organic chemical compound with the formula CH 3 CHO, sometimes abbreviated as Me CHO. It is a colorless liquid or gas, boiling near room temperature. It is one of the most important aldehydes, occurring widely in nature and being produced on a large scale in industry.

  7. 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]

  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. Sagittarius B2 - Wikipedia

    en.wikipedia.org/wiki/Sagittarius_B2

    An ester, ethyl formate, was also discovered, which is a major precursor to amino acids. This ester is also responsible for the flavour of raspberries, [8] leading some articles on Sagittarius B2 to postulate the cloud as smelling of ‘raspberry rum’.