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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)

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4. Sigma-Aldrich - Wikipedia

   en.wikipedia.org/wiki/Sigma-Aldrich

   Sigma Advanced Genetic Engineering (SAGE) Labs is a division within Sigma-Aldrich that specializes in genetic manipulation of in vivo systems for special research and development applications. It was formed in 2008 to investigate zinc finger nuclease technology and its application for disease research models.

5. Acetic acid - Wikipedia

   en.wikipedia.org/wiki/Acetic_acid

   acetyl chloride SOCl 2 acetic acid (i) Li[AlH 4], ether (ii) H 3 O + ethanol Two typical organic reactions of acetic acid Acetic acid undergoes the typical chemical reactions of a carboxylic acid. Upon treatment with a standard base, it converts to metal acetate and water. With strong bases (e.g., organolithium reagents), it can be doubly deprotonated to give LiCH 2 COOLi. Reduction of acetic ...

6. Acetylacetone - Wikipedia

   en.wikipedia.org/wiki/Acetylacetone

   The enzyme acetylacetone dioxygenase cleaves a central carbon-carbon bond of acetylacetone, producing acetate and 2-oxopropanal. The enzyme is iron(II)-dependent, but it has been proven to bind to zinc as well. Acetylacetone degradation has been characterized in the bacterium Acinetobacter johnsonii. [13] CH 3 C(O)CH 2 C(O)CH 3 + O 2 → CH 3 ...

7. List of boiling and freezing information of solvents - Wikipedia

   en.wikipedia.org/wiki/List_of_boiling_and...

   This Wikipedia page provides a comprehensive list of boiling and freezing points for various solvents.

8. 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]

9. Dimethylaminoethyl acrylate - Wikipedia

   en.wikipedia.org/wiki/Dimethylaminoethyl_acrylate

   When ethyl acrylate is used as a reactant, ethanol is formed; this forms with the ethyl acrylate an azeotrope of the composition ethanol/ethyl acrylate 72.7:26.3%, which boils at 77.5 °C under atmospheric pressure. [8] To achieve a high reaction yield, the ethanol is distilled off from the reaction mixture.