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Cyclopenta[c]cyclopropa[g][1,6]diazacyclotetradecine-12a(1H)-carboxylic acid, 2,3,3a,4,5,6,7,8,9,11a,12,13,14,14a-tetradecahydro-2-[[7-Methoxy-8-Methyl-2-[4-(1-Methylethyl)-2-thiazolyl]-4-quinolinyl]oxy]-5-Methyl-4,14-dioxo-, (2R,3aR,10Z,11aS,12aR,14aR)is a complex cyclic organic acid with a unique molecular structure. It features multiple rings and functional groups, including a thiazolyl and quinolinyl moiety, which may suggest potential pharmacological or biological activities.

923604-58-4

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923604-58-4 Usage

Uses

As the provided materials do not specify any particular applications for Cyclopenta[c]cyclopropa[g][1,6]diazacyclotetradecine-12a(1H)-carboxylic acid, 2,3,3a,4,5,6,7,8,9,11a,12,13,14,14a-tetradecahydro-2-[[7-Methoxy-8-Methyl-2-[4-(1-Methylethyl)-2-thiazolyl]-4-quinolinyl]oxy]-5-Methyl-4,14-dioxo-, (2R,3aR,10Z,11aS,12aR,14aR)-, it is not possible to list its uses based on the information given. However, given its complex structure and the presence of various functional groups, it could potentially be explored for applications in pharmaceuticals, materials science, or other fields where novel chemical compounds with unique properties are of interest. Further research and development would be required to determine the specific uses and benefits of Cyclopenta[c]cyclopropa[g][1,6]diazacyclotetradecine-12a(1H)-carboxylic acid, 2,3,3a,4,5,6,7,8,9,11a,12,13,14,14a-tetradecahydro-2-[[7-Methoxy-8-Methyl-2-[4-(1-Methylethyl)-2-thiazolyl]-4-quinolinyl]oxy]-5-Methyl-4,14-dioxo-, (2R,3aR,10Z,11aS,12aR,14aR)- in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 923604-58-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,6,0 and 4 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 923604-58:
(8*9)+(7*2)+(6*3)+(5*6)+(4*0)+(3*4)+(2*5)+(1*8)=164
164 % 10 = 4
So 923604-58-4 is a valid CAS Registry Number.

923604-58-4Downstream Products

923604-58-4Relevant academic research and scientific papers

Ring-Closing Metathesis on Commercial Scale: Synthesis of HCV Protease Inhibitor Simeprevir

Horváth, András,Depre, Dominique,Vermeulen, Wim A. A.,Wuyts, Stijn L.,Harutyunyan, Syuzanna R.,Binot, Grégori,Cuypers, Jef,Couck, Wouter,Den Heuvel, Dirk Van

, p. 4932 - 4939 (2019)

The key macrocyclization step in the synthesis of simeprevir, a hepatitis C virus (HCV) antiviral drug, was studied. N-Boc substitution on the diene precursor changes the site of insertion of the metathesis catalyst and, consequently, the kinetic model of the ring closing metathesis (RCM), enabling a further increase in the macrocyclization efficiency under simulated high dilution (SHD) conditions. NMR of the inserted species of both first and second generation RCM catalysts are reported and discussed.

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