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As a primary haloalkane, it is prone to S N 2 type reactions. It is commonly used as an alkylating agent. When combined with magnesium metal in dry ether, it gives the corresponding Grignard reagent. Such reagents are used to attach butyl groups to various substrates. 1-Bromobutane is the precursor to n-butyllithium: [4] 2 Li + C 4 H 9 X → C ...
1-Bromobutane (n-butyl bromide) 2-Bromobutane (sec-butyl bromide or methylethylbromomethane) This page was last edited on 6 February 2021 ...
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.
Butyl bromide (C 4 H 9 Br) may refer to: 1-Bromobutane (n-Butyl bromide) 2-Bromobutane (sec-butyl bromide) 1-Bromo-2-methylpropane (isobutyl bromide)
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Tetrabutylammonium bromide can be prepared by the alkylation of tributylamine with 1-bromobutane. [2] Tetrabutylammonium bromide is used to prepare other salts of the tetrabutylammonium cation by salt metathesis reactions. [6] It serves as a source of bromide ions for substitution reactions.
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tert-Butyl bromide (also referred to as 2-bromo-2-methylpropane) is an organic compound with the formula Me 3 CBr (Me = methyl). The molecule features a tert-butyl group attached to a bromide substituent. This organobromine compound is used as a standard reagent in synthetic organic chemistry. It is a colorless liquid.