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Butyl chloride (C 4 H 9 Cl) may refer to: n-Butyl chloride (butan-1-chloride) sec-Butyl chloride (butan-2-chloride) Isobutyl chloride (1-chloro-2-methylpropane)
tert-Butyl chloride is the organochloride with the formula (CH 3) 3 CCl. It is a colorless, flammable liquid. It is sparingly soluble in water, with a tendency to undergo hydrolysis to the corresponding tert-butyl alcohol. It is produced industrially as a precursor to other organic compounds. [1]
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In organic chemistry, butyl is a four-carbon alkyl radical or substituent group with general chemical formula −C 4 H 9, derived from either of the two isomers (n-butane and isobutane) of butane. The isomer n -butane can connect in two ways, giving rise to two "-butyl" groups:
N-tert-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. [1] It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions. The nitrogen atom in the resulting intermediate is basic, and can abstract an α-hydrogen to create a new double bond.
Isobutyl chloride (1-chloro-2-methylpropane) is an organochlorine compound. It is a chlorinated derivative of isobutane. Synthesis.
Tetrabutylammonium chloride is the organic compound with the formula [(CH 3 CH 2 CH 2 CH 2) 4 N] + Cl −, often abbreviated as [Bu 4 N]Cl, where Bu stands for n-butyl. A white water-soluble solid, it is a quaternary ammonium salt of chloride. It is a precursor to other tetrabutylammonium salts.
Butyryl chloride is an organic compound with the chemical formula CH 3 CH 2 CH 2 C(O)Cl. It is a colorless liquid with a unpleasant odor. It is a colorless liquid with a unpleasant odor. Butyryl chloride is soluble in organic solvents, but it reacts readily with water and alcohols.