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4946-22-9

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4946-22-9 Usage

Description

4-(Dimethylamino)thiophenol is an organic compound characterized by the presence of a thiophene ring with a dimethylamino group at the 4-position. It is known for its unique chemical properties and potential applications in various fields.

Uses

Used in Pharmaceutical Industry:
4-(Dimethylamino)thiophenol is used as a therapeutic agent for the treatment of various health conditions, including HBV and HDV infections, hypercholesterolemia, diabetes, and cancer. Its application is attributed to its ability to act as NTCP inhibitors, which can help in the treatment and management of these diseases.
Used in Hepatoprotection:
4-(Dimethylamino)thiophenol is used as a hepatoprotective agent, aiming to protect and improve liver function. Its application is based on its potential to ameliorate liver-related conditions and support overall liver health.
Used in Hypercholesterolemia Treatment:
4-(Dimethylamino)thiophenol is used as a cholesterol-lowering agent, particularly for the amelioration of hypercholesterolemia. Its application is due to its ability to help regulate cholesterol levels and improve cardiovascular health.
Used in Diabetes Management:
4-(Dimethylamino)thiophenol is used in the management of diabetes, as it may help in controlling blood sugar levels and improving overall metabolic health.
Used in Cancer Treatment:
4-(Dimethylamino)thiophenol is used as an anticancer agent, potentially inhibiting the growth and progression of cancer cells. Its application in this field is based on its ability to target and interfere with cancer-related pathways, making it a promising candidate for cancer treatment and research.

Check Digit Verification of cas no

The CAS Registry Mumber 4946-22-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4946-22:
(6*4)+(5*9)+(4*4)+(3*6)+(2*2)+(1*2)=109
109 % 10 = 9
So 4946-22-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NS/c1-9(2)7-3-5-8(10)6-4-7/h3-6,10H,1-2H3

4946-22-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(dimethylamino)thiophenol

1.2 Other means of identification

Product number -
Other names 4-(Dimethylamino)benzenethiol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4946-22-9 SDS

4946-22-9Relevant articles and documents

Imposing Latency in Ruthenium Sulfoxide-Chelated Benzylidenes: Expanding Opportunities for Thermal and Photoactivation in Olefin Metathesis

Alassad, Nebal,Goldberg, Israel,Kozuch, Sebastian,Lemcoff, N. Gabriel,Nechmad, Noy B.,Rozenberg, Illya,Segalovich-Gerendash, Gal

, p. 4827 - 4834 (2020/06/01)

Herein we show the design and synthesis of an electron-rich, sulfoxide-chelated, ruthenium benzylidene. In contrast to previously reported sulfoxide-chelated ruthenium benzylidenes, this complex is more stable in a cis-dichloro conformation and is thus latent in typical olefin metathesis reactions. The complex was characterized by NMR, UV-vis, and X-ray spectroscopy, alongside density functional theory computations. The latent precatalyst could be activated thermally and, depending on the solvent, by UV-C or visible light. In addition, an original "thermo-chromatic" orthogonal sequence was developed, further improved by the use of a thioether chelated complex, where a divergent two-step synthesis can lead to a dihydrofuran or a dihydropyran depending only on the order by which the different stimuli, heat or light, are applied.

HISTONE DEACETYLASE INHIBITORS

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Page 49, (2008/06/13)

The present invention provides histone deacetylase inhibitors of general formula (I), process for the preparation of such compounds and uses of the compounds in medicine.

Polymerisation inhibitor

-

, (2008/06/13)

A monomer composition, stabilized against premature polymerization, comprising: a) an ethylenically unsaturated monomer or mixture of monomers polymerizable by free radical initiation, and b) an effective amount, sufficient to inhibit premature polymerization of component (a) of a mixture of: i) 1 to 99% by weight, based on the total weight of components (i) and (ii), of a mixture of at least one aromatic amine and at least one organic acid in a molar ratio of 10:1 to 1:10, and ii) 99 to 1% by weight, based on the total weight of components (i) and (ii), of at least one stable radical compound.

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