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2-Phenethyl propionate, also known as phenethyl propanoate or phenylethyl propionate, [2] is the ester of phenethyl alcohol and propionic acid. It can be found in peanuts. [3] It has shown antifungal activity [4] and was tested as a pesticide. [5] It is used in some preparations used in the management of bed bugs [6] and in other pesticide ...
The CompTox Chemicals Dashboard is a freely accessible online database created and maintained by the U.S. Environmental Protection Agency (EPA). The database provides access to multiple types of data including physicochemical properties, environmental fate and transport, exposure, usage, in vivo toxicity, and in vitro bioassay.
Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH. It is a colourless liquid with a pleasant floral odor. It is a colourless liquid with a pleasant floral odor.
The propionate / ˈ p r oʊ p i ə n eɪ t /, or propanoate, ion is C 2 H 5 COO −, the conjugate base of propionic acid. It is the form found in biological systems at physiological pH. A propionic, or propanoic, compound is a carboxylate salt or ester of propionic acid. In these compounds, propionate is often written in shorthand, as CH 3 CH ...
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.
It is related to the drug MPPP, with an N-phenethyl group in place of the N-methyl substitution and an acetate ester rather than propionate. PEPAP is approximately 6–7 times more potent than morphine in laboratory rats. [1] PEPAP presumably has similar effects to other opioids, producing analgesia, sedation and euphoria.
4-Coumaroyl-CoA is the central biosynthetic precursor to phenylpropanoids (shown in protonated state) Phenylalanine Tyrosine. The phenylpropanoids are a diverse family of organic compounds that are biosynthesized by plants from the amino acids phenylalanine and tyrosine in the shikimic acid pathway. [1]
Phenylpropanoic acid can be prepared from cinnamic acid by hydrogenation. [5] [6] Originally it was prepared by reduction with sodium amalgam in water and by electrolysis.[7]A characteristic reaction of phenylpropanoic acid is its cyclization to 1-indanone.