F 2-Methyl-2-propanethiol

Individually indexed compounds are f Butanethiol, 1712 f 2-Butanethiol, 1713 Dodecanethiol, 3567 f Ethanethiol, 0933 f Methanethiol, 0489 f 2-Methylbutane-2-thiol, 2023 f 3-Methylbutanethiol, 2024 f 2-Methylpropanethiol, 1715 f 2-Methyl-2-propanethiol, 1716... 

Sulfenamides. /er/-Butyl azidoformate added dropwise during 0.5 hr. at room temp, under Ng to a stirred mixture of 2-methyl-2-propanethiol and cuprous diloride, stirring continued 10 hrs. at room temp. N-/er -butoxycarbonyl-2-methyl-2-propanesulfenylamide. Y 77%. - Similarly with tert-hMiy azidoacetate N-fer/-butoxycarbonylmethyl-2-methyl-2-propanesulfenylamide. Y 64%. F. e. and products s. T. Saegusa, Y. Ito, and T. Shimizu, J. Org. Chem. 35, 2979 (1970). 

Three isomers of butyl mercaptan (BYOO-til mer-KAP-tan) exist. Isomers are two or more forms of a chemical compound with the same molecular formula, but different structural formulas and different chemical and physical properties. The names and synonyms of the isomers are n-butyl mercaptan, known as l-hutanethiol, i-mercapto-butane, or n-butyl thioalcohol -butyl mercaptan, called 2-butanethiol or i-methyl-i-propanethiol and ferf-butyl mercaptan, also known as 2-methyl-2-propanethiol. The isomers have slightly different expanded chemical formulas n-butyl mercaptan, CH3CH2CH2CH2SH -butyl mercaptan, CH3CH2CH(SH)CH3 and ferf-butyl mercaptan, CH3C(CH3)(SH)CH3. The isomers have vastly differing melting points n-butyl mercaptan, —115.67 (—i76.2i°F) -butyl mercaptan,... 

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