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1-Bromobutane is the organobromine compound with the formula CH 3 (CH 2) 3 Br. It is a colorless liquid, although impure samples appear yellowish. It is insoluble in water, but soluble in organic solvents. It is primarily used as a source of the butyl group in organic synthesis. It is one of several isomers of butyl bromide.
tert-Butyl bromide used to study the massive deadenylation of adenine based-nucleosides induced by halogenated alkanes (alkyl halides) under physiological conditions. 2-Bromo-2-methylpropane causes the massive deguanylation of guanine based-nucleosides and massive deadenylation of adenine based-nucleosides.
Bromobutane (molecular formula: C 4 H 9 Br, molar mass: 137.02 g/mol) may refer to either of two chemical compounds: 1-Bromobutane ( n -butyl bromide) 2-Bromobutane ( sec -butyl bromide or methylethylbromomethane)
Replacing 1-bromopropane with water or acetone-based adhesives is the preferred NIOSH option for controlling occupational exposure, but other options include engineering controls like isolation and ventilation, administrative controls, and PPE that includes respiratory and skin protection.
The standard preparation for n-BuLi is reaction of 1-bromobutane or 1-chlorobutane with Li metal: [3] 2 Li + C 4 H 9 X → C 4 H 9 Li + LiX (X = Cl, Br) If the lithium used for this reaction contains 1–3% sodium, the reaction proceeds more quickly than if pure lithium is used.
Most 1-bromoalkanes are prepared by free-radical addition of hydrogen bromide to the 1-alkene. These conditions lead to anti-Markovnikov addition, giving the 1-bromo derivative. [2] 1-Bromohexane undergoes reactions expected of simple alkyl bromides. It can form Grignard reagents. [3]
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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.