cas 18906-37-1, 2,4-dimethoxybenzene-1-thiol | Articles data ｜lookchem

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18906-37-1

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Suter,Hansen
p. 2080
(1933)
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Facile introduction of SH group on aromatic substrates via electrophilic substitution reactions
Herein, we describe a mild and efficient two-step procedure to introduce a thiol group on aromatic substrates. First, reaction with an activated sulfoxide leads to an arylsulfonium salt intermediate. Then, two successive β-elimination-based dealkylation reactions afford the desired arylthiols in good to excellent yields.
Becht, Jean-Michel,Wagner, Alain,Mioskowski, Charles
p. 5758 - 5761
(2007/10/03)

Phthalimidesulfenyl chloride. x1. a synthetic equivalent of hs+ and+s-s+ species in electrophilic aromatic substitutions
The reaction of phthalimidesulfenyl chloride, 1, with activated arenes provides monosubstituted phthalimidesulfenyl derivatives 3 which can be easily transformed into the corresponding disulfides 7, thiols 8 and masked thiols 9.
Capozzi, Giuseppe,Falciani, Chiara,Menichetti, Stefano,Nativi, Cristina
p. 227 - 232
(2007/10/03)

Monomethylthio analogues of 1-(2,4,5-trimethoxyphenyl)-2-aminopropane
Regiospecific syntheses of the three monomethylthio analogues of 1-(2,4,5- trimethoxyphenyl)-2-aminopropane are described. The three isomeric amines were evaluated for potential psychotomimetic potency using the rabbit hyperthermia assay. Enantiomeric com
Jacob III,Anderson III,Meshul,Shulgin,Castagnoli Jr.
p. 1235 - 1239
(2007/10/06)

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Chemical Properties

Boiling Point: 278.1 °C at 760 mmHg
Flash Point:122 °C
Density: 1.134 g/cm³
Storage Temp.:2-8°C
Vapor Pressure: 0.00734mmHg at 25°C
Refractive Index: 1.549
PSA: 57.26000
LogP: 1.99250

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