enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Phenylacetone

    Phenylacetone, also known as phenyl-2-propanone, is an organic compound with the chemical formula C 6 H 5 CH 2 COCH 3. It is a colorless oil that is soluble in organic solvents. It is a mono-substituted benzene derivative, consisting of an acetone attached to a phenyl group. As such, its systematic IUPAC name is 1-phenyl-2-propanone.

  3. 3,4-Methylenedioxyphenylpropan-2-one - Wikipedia

    en.wikipedia.org/wiki/3,4-Methylenedioxyphenyl...

    3,4-Methylenedioxyphenylpropan-2-one [1] or piperonyl methyl ketone (MDP2P or PMK) is a chemical compound consisting of a phenylacetone moiety substituted with a methylenedioxy functional group. It is commonly synthesized from either safrole (which, for comparison, is 3-[3,4-(methylenedioxy)phenyl]-2-propene) or its isomer isosafrole via ...

  4. Propiophenone - Wikipedia

    en.wikipedia.org/wiki/Propiophenone

    Propiophenone can be prepared by Friedel–Crafts reaction of propanoyl chloride and benzene.It is also prepared commercially by ketonization of benzoic acid and propionic acid over calcium acetate and alumina at 450–550 °C: [1]

  5. Phenylacetylcarbinol - Wikipedia

    en.wikipedia.org/wiki/Phenylacetylcarbinol

    Synonyms are 1-hydroxy-1-phenyl-2-propanone and 1-Hydroxy-1-phenylacetone. Production. R)-PAC is widely synthesized by fermentation of benzaldehyde and dextrose.

  6. Phenylpropene - Wikipedia

    en.wikipedia.org/wiki/Phenylpropene

    Phenylpropenes broadly are compounds containing a phenyl ring bonded to propene, more specifically those with an allyl group bonded to a benzene ring, having the parent structure of allylbenzene. These comprise a class of phenylpropanoids , where there are typically other substituents bonded to the aromatic ring.

  7. Oxime - Wikipedia

    en.wikipedia.org/wiki/Oxime

    Amidoximes are oximes of amides (R 1 C(=O)NR 2 R 3) with general structure R 1 C(=NOH)NR 2 R 3. Oximes are usually generated by the reaction of hydroxylamine with aldehydes (R−CH=O) or ketones (RR’C=O). The term oxime dates back to the 19th century, a combination of the words oxygen and imine. [1]

  8. How far would a wife go to keep $2M Ponzi scheme a secret? - AOL

    www.aol.com/far-wife-keep-2m-ponzi-110855243.html

    In February 2019, 38-year-old Michael Cochran died suddenly. Prosecutors said his wife Natalie Cochran poisoned him with insulin to conceal her over $2 million Ponzi scheme, which she operated ...

  9. Reductive amination - Wikipedia

    en.wikipedia.org/wiki/Reductive_amination

    Reductive amination (also known as reductive alkylation) is a form of amination that converts a carbonyl group to an amine via an intermediate imine.The carbonyl group is most commonly a ketone or an aldehyde.