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Neopentyl alcohol was the first described in 1891 by L. Tissier, who prepared it by reduction of a mixture of trimethyl acetic acid and trimethylacetyl chloride with sodium amalgam. [ 4 ] Neopentyl alcohol can be converted to neopentyl iodide by treatment with triphenylphosphite / methyl iodide : [ 5 ]
or isoamyl alcohol or isopentyl alcohol primary 3-Methylbutan-1-ol: 131.2 2,2-dimethyl-1-propanol or neopentyl alcohol primary 2,2-Dimethylpropan-1-ol: 113.1 2-pentanol or sec-amyl alcohol or methyl (n) propyl carbinol secondary Pentan-2-ol: 118.8 3-methyl-2-butanol or sec-isoamyl alcohol or methyl isopropyl carbinol secondary 3-Methylbutan-2 ...
This list is ordered by the number of carbon atoms in an alcohol. C1. Methanol; C2. Ethanol; C3 ... Isoamyl alcohol; 2-Methyl-1-butanol; Neopentyl alcohol; 2-Pentanol;
Neopentyl alcohol; Neopentylamine; Neopentyllithium; Nirogacestat This page was last edited on 24 March 2024, at 14:31 (UTC). Text is available under the Creative ...
uses, rubbing alcohol is an inexpensive, drugstore wallflower worth a second look. Priced to sell between $1.99 (CVS for 70% Isopropyl) and $3.95 for ...
A neopentyl substituent, often symbolized by "Np", has the structure Me 3 C–CH 2 – for instance neopentyl alcohol (Me 3 CCH 2 OH or NpOH). As Np also symbolises the element neptunium (atomic number 93) one should use this abbreviation with care. The obsolete name tetramethylmethane is also used, especially in older sources. [8] [9]
Conversely, the name pentyl was used for several five-carbon branched alkyl groups, distinguished by various prefixes. The nomenclature has now reversed, with "amyl" being more often used to refer to the terminally branched group also called isopentyl, as in amobarbital. A cyclopentyl group is a ring with the formula -C 5 H 9.
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