874534-90-4 Usage
Uses
Used in Pharmaceutical Industry:
Heptanedioic acid, 2-methylene-6-[[(phenylmethoxy)carbonyl]amino]-, 7-methyl ester, (6S)is used as a potential pharmaceutical agent for its unique structural features. Heptanedioic acid, 2-methylene-6-[[(phenylmethoxy)carbonyl]amino]-,
7-methyl ester, (6S)-'s specific stereochemistry and functional groups may contribute to its biological activity, making it a candidate for the development of new drugs or therapeutic agents. Its application in this industry could be for targeting specific diseases or conditions, depending on its pharmacological profile.
Used in Organic Synthesis:
In the field of organic synthesis, Heptanedioic acid, 2-methylene-6-[[(phenylmethoxy)carbonyl]amino]-, 7-methyl ester, (6S)can be utilized as a building block or intermediate in the synthesis of more complex organic molecules. Its unique structural elements, including the methylene group and phenylmethoxy carbonyl amino group, may facilitate the formation of new chemical entities with novel properties and applications.
Further research and testing are necessary to fully understand the properties and potential uses of Heptanedioic acid, 2-methylene-6-[[(phenylmethoxy)carbonyl]amino]-,
7-methyl ester, (6S)- in various industries. Its unique structural features and stereochemistry may offer new opportunities for the development of innovative products and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 874534-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,4,5,3 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 874534-90:
(8*8)+(7*7)+(6*4)+(5*5)+(4*3)+(3*4)+(2*9)+(1*0)=204
204 % 10 = 4
So 874534-90-4 is a valid CAS Registry Number.
874534-90-4Relevant academic research and scientific papers
The stereoselective synthesis of aziridine analogues of diaminopimelic acid (DAP) and their interaction with dap epimerase
Diaper, Christopher M.,Sutherland, Andrew,Pillai, Bindu,James, Michael N.G.,Semchuk, Paul,Blanchard, John S.,Vederas, John C.
, p. 4402 - 4411 (2007/10/03)
Aziridine analogues of diaminopimelic acid (DAP) have been prepared stereoselectively for the first time and evaluated as inhibitors of DAP epimerase. (2R,3S,3′S)-3-(3′-Aminopropane)aziridine-2,3′- dicarboxylate 4 was synthesised and shown to be a reversible inhibitor of DAP epimerase with an IC50 value of 2.88 mM. (2S,4S)- and (2S,4R)-2-(4-Amino-4-carboxybutyl)aziridine-2-carboxylic acid (LL-azi-DAP 14 and DL-azi-DAP 29) were made as pure diastereomers, and both were shown to be irreversible inhibitors of DAP epimerase. LL-Azi-DAP 14 selectively binds to Cys-73 of the enzyme active site whereas DL-azi-DAP 29 binds to Cys-217 via attack of sulfhydryl on the methylene of the inhibitor aziridine ring. These observations are consistent with the two base mechanism proposed for the epimerisation of LL-DAP 1 and meso-DAP 2 by DAP epimerase. The Royal Society of Chemistry 2005.
