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[(4-METHOXY-PHENYLCARBAMOYL)-METHYLSULFANYL]-ACETIC ACID is a complex organic molecule that features a phenyl group connected to a carbamoyl and methylsulfanyl group, all attached to an acetic acid molecule. [(4-METHOXY-PHENYLCARBAMOYL)-METHYLSULFANYL]-ACETIC ACID may hold potential applications in the pharmaceutical industry, given the presence of the carbamoyl group, which could play a role in drug development or serve as a chemical intermediate in organic synthesis. Further research and analysis are necessary to determine the specific properties and potential uses of [(4-METHOXY-PHENYLCARBAMOYL)-METHYLSULFANYL]-ACETIC ACID.

338409-65-7

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338409-65-7 Usage

Uses

Used in Pharmaceutical Industry:
[(4-METHOXY-PHENYLCARBAMOYL)-METHYLSULFANYL]-ACETIC ACID is used as a potential candidate in drug development for its carbamoyl group, which may contribute to the creation of new pharmaceutical compounds.
Used in Organic Synthesis:
[(4-METHOXY-PHENYLCARBAMOYL)-METHYLSULFANYL]-ACETIC ACID is used as a chemical intermediate in organic synthesis, where its unique structure can be utilized to synthesize other complex molecules for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 338409-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,8,4,0 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 338409-65:
(8*3)+(7*3)+(6*8)+(5*4)+(4*0)+(3*9)+(2*6)+(1*5)=157
157 % 10 = 7
So 338409-65-7 is a valid CAS Registry Number.

338409-65-7Downstream Products

338409-65-7Relevant academic research and scientific papers

Synthesis and dynamic stereochemistry of 4-aryl-thiomorpholine-3,5-dione derivatives

Szawka?o, Joanna,Maurin, Jan K.,Pluciński, Franciszek,Czarnocki, Zbigniew

, p. 383 - 390 (2014/12/10)

A series of new N-aryl-substituted thiomorpholine-3,5-diones were synthesized. Crystal structures of seven compounds were established on the basis of X-ray crystallography. Stable at room temperature diastereomers were detected for (2-phenyl)-substituted derivatives using 1H NMR. The dynamic stereochemistry of compound 36 was studied with variable-temperature 1H NMR and the mechanism of diastereomers interconversion was proposed on the basis of quantum chemical calculations.

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