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2-Phenylphenol is a precursor to 9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, a commercial fire retardant. The sodium salt of orthophenyl phenol, sodium orthophenyl phenol, is a preservative, used to treat the surface of citrus fruits. [5] Orthophenyl phenol is also used as a fungicide in food packaging and may migrate into the contents. [6]
o-Phenylphenol, sodium; Sodium o-phenylphenol; Sodium 2-phenylphenolate; Sodium o-phenylphenate; Identifiers CAS Number. 132-27-4 ...
Phenol in the Berthelot reagent can be replaced by a variety of phenolic reagents, the most common being sodium salicylate, which is significantly less toxic. [1] This has been used for blood urea nitrogen (BUN) determinations and commonly is used to determine water and soil total and ammonia-N. Replacement of phenol by 2-phenylphenol reduces interferences by a variety of soil and water ...
This is a list of fungicides.These are chemical compounds which have been registered as agricultural fungicides.The names on the list are the ISO common name for the active ingredient which is formulated into the branded product sold to end-users. [1]
2-Phenylphenol. Sodium 2-phenylphenol; 4-Phenylphenol This page was last edited on 9 November 2022, at 20:43 (UTC). Text is available under the Creative Commons ...
2 is added with H 2 SO 4 to form phenol (Hock process). In addition to the reactions above, many other more specialized reactions produce phenols: rearrangement of esters in the Fries rearrangement [7] [8] rearrangement of N-phenylhydroxylamines in the Bamberger rearrangement [9] [10] dealkylation of phenolic ethers; reduction of quinones
2-Phenylphenol, or o-phenylphenol; 4-Phenylphenol, or p-phenylphenol This page was last edited on 10 June 2023, at 00:21 (UTC). Text is available under the ...
It is generally considered an inductively withdrawing group (-I), because of the higher electronegativity of sp 2 carbon atoms, and a resonance donating group (+M), due to the ability of its π system to donate electron density when conjugation is possible. [5] The phenyl group is hydrophobic. Phenyl groups tend to resist oxidation and reduction.