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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). ?) 2,4,6-Tribromophenol (TBP) is a brominated derivative of phenol. It is used as a fungicide, as a wood preservative, and an intermediate in the preparation of flame retardants.
Bromophenol. A bromophenol is an organic compound consisting of hydroxyl groups and bromine atoms bonded to a benzene ring. They may be viewed as hydroxyl derivatives of bromobenzene, or as brominated derivatives of phenol. There are five basic types of bromophenols (mono- to pentabromophenol) and 19 different bromophenols in total when ...
2,4,6-Tribromoanisole (TBA) is a chemical compound that is a brominated derivative of anisole. It is one of the chemicals responsible for cork taint. [2] Tribromoanisole is a fungal metabolite of 2,4,6-tribromophenol, which is used as a fungicide. It can be found in minute traces on packaging materials stored in the presence of fiberboard ...
Presence of unsaturation and/or phenol or aniline in the sample is shown by disappearance of the deep brown coloration of bromine when it has reacted with the unknown sample. The formation of a brominated phenol (i.e. 2,4,6-tribromophenol ) or aniline (i.e. 2,4,6-tribromoaniline ) in form of a white precipitate indicates that the unknown was a ...
Properties. 2,4,6-Tri- tert -butylphenol is a white solid which dissolves in many organic solvents, but not in aqueous or alcoholic alkaline solutions. The green-blue coloring with iron (III)chloride, which is characteristic for phenols, does not occur in 2,4,6-TTBP. The compound is oxidizable in air but practically non-biodegradable.
Reaction type. Substitution reaction. Identifiers. RSC ontology ID. RXNO:0000072. The Reimer–Tiemann reaction is a chemical reaction used for the ortho - formylation of phenols. [1] [2][3][4] with the simplest example being the conversion of phenol to salicylaldehyde. The reaction was first reported by Karl Reimer and Ferdinand Tiemann.
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The Raschig–Hooker process is a chemical process for the production of chlorobenzene and phenol. [1][2] The Raschig–Hooker process was patented by Friedrich Raschig, a German chemist and politician also known for the Raschig process, the Olin Raschig process and the Raschig ring. [3] He first begun to use this reaction in 1891 in order to ...