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(S)-Methyl 2-(1,3-dioxoisoindolin-2-yl)-3-(4-hydroxy-3-nitrophenyl)propanoate is a complex organic compound with the molecular formula C18H14N2O8. It is a chiral molecule, with the "S" prefix indicating that it has the (S)-configuration at the chiral center. (S)-methyl 2-(1,3-dioxoisoindolin-2-yl)-3-(4-hydroxy-3-nitrophenyl)propanoate features a 1,3-dioxoisoindoline-2-yl group, which is a cyclic structure with two oxygen atoms in a 1,3-relationship, and a 4-hydroxy-3-nitrophenyl group, which contains a hydroxyl group and a nitro group on a phenyl ring. The molecule is characterized by its unique arrangement of functional groups, which may contribute to its potential applications in various chemical or pharmaceutical contexts. Due to its specific stereochemistry and functional groups, it could be relevant in the synthesis of certain drugs or as a building block in organic chemistry.

3116-90-3

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3116-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3116-90-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3116-90:
(6*3)+(5*1)+(4*1)+(3*6)+(2*9)+(1*0)=63
63 % 10 = 3
So 3116-90-3 is a valid CAS Registry Number.

3116-90-3Downstream Products

3116-90-3Relevant academic research and scientific papers

Rhodium(III)-Catalyzed C6-Selective Arylation of 2-Pyridones and Related Heterocycles Using Quinone Diazides: Syntheses of Heteroarylated Phenols

Das, Debapratim,Poddar, Puja,Maity, Saurabh,Samanta, Rajarshi

, p. 3612 - 3621 (2017)

An efficient, direct C6-arylation of 2-pyridones has been successfully accomplished with quinone diazides under Rh(III)-catalyzed redox-neutral conditions. The optimized method is simple, mild, and highly regioselective with a broad substrate scope. The s

Calcilytic compounds

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, (2008/06/13)

Novel calcilytic compounds, pharmaceuticals compositions cotaining said compounds and their use as calcium receptor antagonists.

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