93681-53-9 Usage
Uses
Used in Organic Synthesis:
Benzamide, N-[2-(ethylthio)phenyl]is used as a building block in organic synthesis for creating various pharmaceutical compounds and agrochemicals. Its structure and properties make it suitable for the development of potential drug candidates with diverse biological activities.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Benzamide, N-[2-(ethylthio)phenyl]is used as a key component in the synthesis of new drug candidates. Its unique structure allows for the exploration of different chemical modifications, potentially leading to the discovery of novel therapeutic agents.
Used in Materials Science:
Benzamide, N-[2-(ethylthio)phenyl]may also have potential applications in materials science due to its unique structure and reactivity. It could be utilized in the development of new materials with specific properties, such as improved stability or enhanced reactivity.
Used in Agricultural Research:
In agricultural research, Benzamide, N-[2-(ethylthio)phenyl]could be explored for its potential use in the development of new agrochemicals. Its chemical properties may contribute to the creation of more effective and environmentally friendly pesticides or other agricultural products.
Check Digit Verification of cas no
The CAS Registry Mumber 93681-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,6,8 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 93681-53:
(7*9)+(6*3)+(5*6)+(4*8)+(3*1)+(2*5)+(1*3)=159
159 % 10 = 9
So 93681-53-9 is a valid CAS Registry Number.
93681-53-9Relevant academic research and scientific papers
Diverse Visible-Light-Promoted Functionalizations of Benzotriazoles Inspired by Mechanism-Based Luminescence Screening
Teders, Michael,Gómez-Suárez, Adrián,Pitzer, Lena,Hopkinson, Matthew N.,Glorius, Frank
supporting information, p. 902 - 906 (2017/01/13)
Three new visible-light-promoted functionalizations of benzotriazole substrates were discovered using a mechanism-based screening method. ortho-Thiolated, borylated, and alkylated N-arylbenzamide products were obtained under mild reaction conditions in a new denitrogenative synthetic approach to functionalized aniline derivatives. The functional group tolerance of the borylation reaction was further analyzed in the first application of an additive-based robustness screen in a photocatalytic transformation. All the functionalizations proceed via photocatalytically initiated chain mechanisms as indicated by determination of the reaction quantum yields and Stern–Volmer analyses.
Synthesis of 4H-1,4-Benzothiazines via Lithiation Alpha to Sulphur of 2-Acylaminophenyl Alkyl Sulphides, Sulphoxides, and Sulphones
Babudri, Francesco,Florio, Saverio,Vitrani, Anna Maria,Nunno, Leonardo Di
, p. 1899 - 1903 (2007/10/02)
4H-1,4-Benzothiazines, their monoxides, and their dioxides are readily prepared via lithiation and intramolecular cyclisation of 2-acylaminophenyl alkyl sulphides, sulphoxides, and sulphones with lithium di-isopropylamide in tetrahydrofuran at -50 deg C.
