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  2. Ethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetate

    Ethyl acetate (systematically ethyl ethanoate, commonly abbreviated EtOAc, ETAC or EA) is the organic compound with the formula CH 3 CO 2 CH 2 CH 3, simplified to C 4 H 8 O 2.This flammable, colorless liquid has a characteristic sweet smell (similar to pear drops) and is used in glues, nail polish removers, and the decaffeination process of tea and coffee.

  3. Ethyl acetate (data page) - Wikipedia

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

    for Ethyl Acetate/Water [3] P = 760 mmHg BP Temp. °C % by mole C 4 H 8 O 2; liquid vapor 100.0: 0.0: ... (in ethyl), 7.1 Hz. MS; Masses of main fragments 88.0 (5.1% ...

  4. Triethyl phosphonoacetate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphonoacetate

    Triethyl phosphonoacetate is a reagent for organic synthesis used in the Horner-Wadsworth-Emmons reaction (HWE) or the Horner-Emmons modification.. Triethyl phosphonoacetate can be added dropwise to sodium methoxide solution to prepare a phosphonate anion.

  5. 2-Ethoxyethanol - Wikipedia

    en.wikipedia.org/wiki/2-Ethoxyethanol

    2-Ethoxyethanol, also known by the trademark Ethyl cellosolve, is a solvent used widely in commercial and industrial applications. It is a clear, colorless, nearly odorless liquid that is miscible with water, ethanol, diethyl ether, acetone, and ethyl acetate. [3] 2-Ethoxyethanol is manufactured by the reaction of ethylene oxide with ethanol.

  6. 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. As a carbene precursor, it is used in the cyclopropanation of alkenes.

  7. Ethyl acetoacetate - Wikipedia

    en.wikipedia.org/wiki/Ethyl_acetoacetate

    At large scale, ethyl acetoacetate is industrially produced by treatment of diketene with ethanol. [2] The small scale preparation of ethyl acetoacetate is a classic laboratory procedure. [3] It involves Claisen condensation of ethyl acetate. Two moles of ethyl acetate condense to form one mole each of ethyl acetoacetate and ethanol. [4]

  8. Propanephosphonic acid anhydride - Wikipedia

    en.wikipedia.org/wiki/Propanephosphonic_acid...

    CAS Number. 68957-94-8; 3D model ... [1] The chemical is a ... It is commercially available as 50 % solution in DMF or ethyl acetate as a slightly yellow mixture.

  9. Phenethyl acetate - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_acetate

    Phenethyl acetate is the ester resulting from the condensation of acetic acid and phenethyl alcohol. Like many esters, it is found in a range of fruits and biological products. [ 1 ] It is a colorless liquid with a rose and honey scent and a raspberry-like taste.

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