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Ethanethione, 2-(2-chlorophenyl)-1-(4-Morpholinyl)is a chemical compound characterized by the molecular formula C12H15ClNOS. It is a thioether derivative that features a chlorophenyl and morpholinyl functional group, which contributes to its unique chemical properties and potential applications.
Used in Medicinal Chemistry and Pharmaceutical Research:
Ethanethione, 2-(2-chlorophenyl)-1-(4-Morpholinyl)is utilized as a key component in medicinal chemistry and pharmaceutical research. Its unique structure and functional groups make it a valuable target for the development of new drug candidates and therapeutic agents.
Used in Drug Development:
In the pharmaceutical industry, Ethanethione, 2-(2-chlorophenyl)-1-(4-Morpholinyl)is used as a precursor or building block in the synthesis of potential drug candidates. Its chemical properties allow for the creation of novel compounds with potential therapeutic effects for the treatment of various diseases and conditions.
Used in the Treatment of Various Diseases and Conditions:
Ethanethione, 2-(2-chlorophenyl)-1-(4-Morpholinyl)has potential applications in the treatment of a range of diseases and conditions. Its unique structure and functional groups may contribute to the development of new therapeutic agents with improved efficacy and selectivity.
Overall, Ethanethione, 2-(2-chlorophenyl)-1-(4-Morpholinyl)is a promising chemical compound with a wide range of potential applications in the fields of medicinal chemistry, pharmaceutical research, and drug development. Its unique structure and functional groups make it a valuable target for further study and synthesis of related compounds with potential therapeutic properties.

159298-85-8

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159298-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159298-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,2,9 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 159298-85:
(8*1)+(7*5)+(6*9)+(5*2)+(4*9)+(3*8)+(2*8)+(1*5)=188
188 % 10 = 8
So 159298-85-8 is a valid CAS Registry Number.

159298-85-8Downstream Products

159298-85-8Relevant academic research and scientific papers

Synthesis of 2-aminobenzo[b]thiophenes from 4-(2-haloaryl)-1,2,3-thiadiazoles

Androsov,Popova,Petrov,Ponyaev

, p. 2405 - 2408 (2014)

A new approach to the synthesis of 2-aminobenzo[b]thiophenes was developed on the basis of reaction of 4-aryl-1,2,3-thiadiazoles with amines in the presence of potassium carbonate. The effect of the nature of substituent in the benzene ring of the starting 4-aryl-1,2,3-thiadiazoles on the structure of the final product was studied.

Preparation method of phenyl crotonic acid ester compound

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Paragraph 0030-0032; 0036; 0056-0057, (2021/05/19)

The invention relates to the technical field of organic synthesis, in particular to a preparation method of a phenyl crotonate compound, the preparation method comprises the following steps: S1, carrying out Willgerodt-Kindler reaction on an acetophenone

A Convenient Approach to 2-Aminobenzo[b]chalcogenophenes Based on Copper-Catalyzed Transformation of 4-(2-Bromophenyl)-1,2,3-chalcogenodiazoles in the Presence of a Base and Amines

Popova,Lyapunova,Petrov,Panikorovskii,Androsov

, p. 689 - 699 (2018/06/14)

The reactions of 4-(2-bromophenyl)-1,2,3-thia-and -selenadiazoles with amines in the presence of potassium carbonate and copper(I) iodide afforded 2-aminobenzo[b]chalcogenophenes. The corresponding thiaand selenamides, prepared by interaction of 4-(2-brom

Selective reduction of carbonyl groups in the presence of low-valent titanium reagents

Lin, Wei,Hu, Ming-Hua,Feng, Xian,Fu, Lei,Cao, Cheng-Pao,Huang, Zhi-Bin,Shi, Da-Qing

, p. 2238 - 2242 (2014/04/17)

The chemoselective reduction of several structurally diverse compounds containing carbonyl groups was achieved in the presence of low-valent titanium reagents. This novel synthetic method provides easy access to highly selective reduction of carbonyl groups, and possesses several advantages including one-step procedure, convenient manipulation, good to excellent yields, and short reaction times.

Ultrasound-mediated willgerodt-kindler reactions: Non-thermal synthesis of thioacetamides

Mojtahedi, Mohammad M.,Alishiri, Tooba,Abaee, M. Saeed

experimental part, p. 1910 - 1915 (2011/10/08)

Non-thermal, solvent-free condensation of several aryl methyl ketones with amines and elemental sulfur is efficiently conducted using ultrasonic irradiation within short time periods. Consequently, various thioacetamides are conveniently synthesized. Simi

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