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  2. Phenylacetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Phenylacetaldehyde

    Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds. It has a role as a human metabolite, a Saccharomyces cerevisiae metabolite, an Escherichia coli metabolite and a mouse metabolite. It is an alpha-CH2-containing aldehyde and a member of ...

  3. Dimethylacetamide - Wikipedia

    en.wikipedia.org/wiki/Dimethylacetamide

    Dimethylacetamide (DMAc or DMA) is the organic compound with the formula CH 3 C(O)N(CH 3) 2. This colorless, water-miscible, high-boiling liquid is commonly used as a polar solvent in organic synthesis. DMA is miscible with most other solvents, although it is poorly soluble in aliphatic hydrocarbons.

  4. Acetaldehyde - Wikipedia

    en.wikipedia.org/wiki/Acetaldehyde

    Conversion of acetaldehyde to 1,1-diethoxyethane, R 1 = CH 3 R 2 = CH 3 CH 2. Acetaldehyde forms a stable acetal upon reaction with ethanol under conditions that favor dehydration. The product, CH 3 CH(OCH 2 CH 3) 2, is formally named 1,1-diethoxyethane but is commonly referred to as "acetal". [39]

  5. Ozonolysis - Wikipedia

    en.wikipedia.org/wiki/Ozonolysis

    CH 3 (CH 2) 7 CH=CH(CH 2) 7 CO 2 H} + 4 O 3 → HO 2 C(CH 2) 7 CO 2 H} + CH 3 (CH 2) 7 CO 2 H. Erucic acid is a precursor to brassylic acid, a C13-dicarboxylic acid that is used to make specialty polyamides and polyesters. The conversion entails ozonolysis, which selectively cleaves the C=C bond in erucic acid: [21]

  6. Dimethoxymethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxymethane

    It has a chloroform-like odor and a pungent taste. It is the dimethyl acetal of formaldehyde. Dimethoxymethane is soluble in three parts water [clarification needed] and miscible with most common organic solvents.

  7. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents. The molecule of phenethyl alcohol consists of a phenethyl group (C 6 H 5 CH 2 CH 2 −) attached to a hydroxyl group ...

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    mail.aol.com

    Get AOL Mail for FREE! Manage your email like never before with travel, photo & document views. Personalize your inbox with themes & tabs. You've Got Mail!

  9. 3-Hydroxybutanal - Wikipedia

    en.wikipedia.org/wiki/3-Hydroxybutanal

    Hydrogenation of 3-hydroxybutanal gives 1,3-butanediol: CH 3 CH(OH)CH 2 CHO + H 2 → CH 3 CH(OH)CH 2 CH 2 OH. This diol is a precursor to 1,3-butadiene, precursor to diverse polymers. Polymerization of 3-hydroxybutanal is also spontaneous, but can be stopped with the addition of water. Aldol has been used in making perfumes and in ore ...