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A series of studies have shown that bromophenols derived from brominated flame retardants (BFRs) in human environments are present in human blood and breast milk. [1] Bromophenols (as well as PBDEs ) were detected in 88% of samples, with 2,4,6-Tribromophenol present in 84% of breast milk samples alone.
1-Bromobutane is the precursor to n-butyllithium: [4] 2 Li + C 4 H 9 X → C 4 H 9 Li + LiX where X = Cl, Br. The lithium for this reaction contains 1-3% sodium. When bromobutane is the precursor, the product is a homogeneous solution, consisting of a mixed cluster containing both LiBr and LiBu.
Bromoform was discovered in 1832 by Löwig who distilled a mixture of bromal and potassium hydroxide, as analogous to preparation of chloroform from chloral. [5]Bromoform can be prepared by the haloform reaction using acetone and sodium hypobromite, by the electrolysis of potassium bromide in ethanol, or by treating chloroform with aluminium bromide.
4-Bromophenylacetic acid is a chemical that can be purchased. [5] Plant protoplasts conjugate aspartic acid with 4-bromophenylacetic acid to form 4-bromophenylacetyl-L-aspartic acid. [2] 4-Bromophenylacetic acid reacts with sodium tetraphenylborate to form felbinac which can be further converted to xenbucin. [4]
95-56-7: 591-20-8: 106-41-2 PubChem ID CID 7244 from PubChem: CID 11563 from PubChem: CID 7808 from PubChem: Chemical formula: C 6 H 5 BrO Molar mass: 173.02 g/mol 1 ...
2-Bromobutane is an isomer of 1-bromobutane. Both compounds share the molecular formula C 4 H 9 Br. 2-Bromobutane is also known as sec-butyl bromide or methylethylbromomethane. Because it contains bromine, a halogen, it is part of a larger class of compounds known as alkyl halides. It is a colorless liquid with a pleasant odor.
(2-Bromophenyl)diphenylphosphine is an organophosphorus compound with the formula (C 6 H 4 Br)P(C 6 H 5) 2. It is a white crystalline solid that is soluble in nonpolar organic solvents. The compound is used as a precursor to the 2-lithiated derivative of triphenylphosphine, [1] which in turn is a precursor to other phosphine ligands.
Bromobenzene is used to introduce a phenyl group into other compounds. One method involves its conversion to the Grignard reagent , phenylmagnesium bromide . This reagent can be used, e.g. in the reaction with carbon dioxide to prepare benzoic acid . [ 4 ]