5977-99-1 Usage
Description
2-Anilinoethanethiol, with the molecular formula C8H11NS, is a chemical compound characterized by its yellowish to brownish liquid appearance and a pungent odor. It is recognized for its strong nucleophilic properties, which allow it to participate in various chemical reactions, leading to the formation of a broad spectrum of derivatives. 2-anilinoethanethiol is primarily utilized as an intermediate in the synthesis of dyes, pharmaceuticals, and organic chemicals, and also finds applications in corrosion inhibition and polymer stabilization. Moreover, 2-anilinoethanethiol has been investigated for its potential in electrochemical and biological fields. However, due to its harmful nature upon ingestion, inhalation, or skin absorption, and its potential to cause irritation and allergic reactions, careful handling and storage are essential.
Uses
Used in Chemical Synthesis Industry:
2-Anilinoethanethiol is used as an intermediate for the production of dyes, pharmaceuticals, and organic chemicals, leveraging its strong nucleophilic properties to facilitate the formation of a wide range of derivatives.
Used in Corrosion Inhibition:
2-Anilinoethanethiol is employed as a corrosion inhibitor, serving to protect materials from the damaging effects of corrosive agents, thereby extending the service life of various industrial components.
Used in Polymer Stabilization:
As a stabilizer for polymers, 2-anilinoethanethiol helps to prevent or reduce the degradation of polymeric materials, maintaining their structural integrity and performance over time.
Used in Electrochemical Applications:
2-Anilinoethanethiol has been studied for its potential role in electrochemical applications, where its unique chemical properties may contribute to advancements in areas such as energy storage and conversion.
Used in Biological Applications:
2-anilinoethanethiol is also being explored for its possible applications in biological research and development, potentially offering new insights or solutions in various biological processes and systems.
Check Digit Verification of cas no
The CAS Registry Mumber 5977-99-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,7 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5977-99:
(6*5)+(5*9)+(4*7)+(3*7)+(2*9)+(1*9)=151
151 % 10 = 1
So 5977-99-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NS/c10-7-6-9-8-4-2-1-3-5-8/h1-5,9-10H,6-7H2
5977-99-1Relevant articles and documents
Oligomerisation reactions of beta substituted thiols in water
Levin, Efrat,Anaby, Aviel,Diesendruck, Charles E.,Berkovich-Berger, Dvora,Fuchs, Benzion,Lemcoff, N. Gabriel
, p. 1735 - 1738 (2013/03/13)
Beta substituted thiols and various derivatives containing the HX-C-C-SH motif oligomerise in water, preferably in the presence of a carbonate salt. The reaction yields oligomers consisting of one thiol end group, a thiaethylene backbone and an additional terminal group corresponding to the starting material used. Mechanistic studies, as well as the scope of substrates and products of these new promising condensation processes, are presented. In addition, strong nucleophiles were also reacted with mercaptoethanol under simple reaction conditions, leading to the selective formation of more complex molecules.
Syntheses de β-sultames (thiazetidines-1,2 dioxyde-1,1)
Champseix, A.,Chanet, J.,Etienne, A.,Berre, A. Lemasson, J. C.,Napierala, C.,Vessiere, R.
, p. 463 - 472 (2007/10/02)
β-sultams (1,2-thiazetidine-1,1-dioxides) are easily prepared by 1-halogensulphonyl-2-aminoalkane cyclisation. Two processes based upon this principle have permitted the preparation of many variously N and C-substituted β-sultams. 1) In the first method 1-chlorosulphonyl-2-aminoalkane hydrochlorides, prepared from taurines or β-aminothiols, cyclised in the presence of base. 2) The second process involves the spontaneous cyclisation of 1-fluorosulphonyl-2-aminoalkanes prepared Michael addition of primary amines to 1-fluorosulphonylethene.
