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2-Aminothiophenol is an organosulfur compound with the formula C 6 H 4 (SH)(NH 2). It is a colorless oily solid, although impure samples can be deeply colored. It is soluble in organic solvents and in basic water. 2-Aminothiophenol is a precursor to benzothiazoles, some of which are bioactive or are commercial dyes.
Thieme Synthesis: [8] Patents (Ex 3): [9] [10] [11]. Thioether formation between 2-Aminothiophenol (1) and 4-Chloro-N,N-Dimethyl-3-Nitrobenzenesulfonamide [137-47-3 ...
Aminothiophenol may refer to: 2-Aminothiophenol; 3-Aminothiophenol [Wikidata] 4-Aminothiophenol This page was last edited on 14 May 2022, at ...
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2-Aminophenol has a variety of uses. As a reducing agent, it is marketed under the names of Atomal and Ortol to develop black-and-white photographs. [3] 2-Aminophenol is an intermediate in the synthesis of dyes. It is particularly useful in yielding metal-complex dyes when diazotized and coupled to a phenol, naphthol, or other aromatic or ...
Hydrolysis of this Herz salt give the corresponding sodium thiolate, which can be further converted to the 2-aminothiophenol. [1] Herz-reaction. The 2-aminothiophenols are suitable for diazotization, giving benzothiadiazoles. [2] Instead the sodium 2-aminothiophenolate can be converted to a 1,3-benzothiazole. Herz-reaction application
This is “the same mechanism targeted by new prescription drugs in Alzheimer’s disease,” he says. Vitamin D might also slow the buildup of tau tangles, which are another hallmark of Alzheimer ...
Benzyl alcohol is used as a bacteriostatic preservative at low concentration in intravenous medications, cosmetics, and topical drugs. [11] Some caution is necessary if a high percent of benzyl alcohol is used as benzaldehyde arises from benzyl alcohol when used as preservative in an injectable formulation solution. [11] [12]
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