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Ethyl 5-acetyl-3-ethyl-4-methyl-1H-pyrrole-2-carboxylate is a complex organic compound with the molecular formula C12H17NO3. It is a derivative of pyrrole, a heterocyclic aromatic organic compound consisting of a five-membered ring with four carbon atoms and one nitrogen atom. In this specific compound, the pyrrole ring is substituted with an acetyl group at the 5-position, an ethyl group at the 3-position, and a methyl group at the 4-position. The molecule also contains an ester functional group, with the carboxylate group attached to the 2-position of the pyrrole ring and an ethyl group as the esterifying agent. ethyl 5-acetyl-3-ethyl-4-methyl-1H-pyrrole-2-carboxylate is likely to be used in the synthesis of various pharmaceuticals, agrochemicals, or other specialty chemicals due to its unique structure and functional groups.

4949-59-1

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4949-59-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4949-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,4 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4949-59:
(6*4)+(5*9)+(4*4)+(3*9)+(2*5)+(1*9)=131
131 % 10 = 1
So 4949-59-1 is a valid CAS Registry Number.

4949-59-1Downstream Products

4949-59-1Relevant academic research and scientific papers

Anion binding modes in meso -substituted hexapyrrolic calix[4]pyrrole isomers

Chang, Kai-Chi,Minami, Tsuyoshi,Koutnik, Petr,Savechenkov, Pavel Y.,Liu, Yuanli,Anzenbacher, Pavel

, p. 1520 - 1525 (2014)

We report on the synthesis of a new receptor for anions, meso-substituted hexapyrrolic calix[4]pyrrole 1. The calix[4]pyrrole's core features two additional pyrrole side-arms suspended above or below the calix[4]pyrrole core. This hexapyrrolic calix[4]pyrrole 1 is formed as cis- and trans-configurational isomers, the structures of which have been determined by single crystal X-ray diffraction. The anion binding experiments revealed interesting difference in the binding mode: The cis-1 isomer binds anions in a mixed binding mode featuring a combination of hydrogen bonding and anion-π interactions resulting in an unexpected strong binding. On the other hand, the trans-1 isomer displays only hydrogen bonding and lower affinity for anions. This is unexpected as one would assume both isomers to display the same binding modes. Overall, the titrations of 1 using UV spectrophotometry and NMR titrations by anions reveal that cis-isomer 1 displays higher affinity (105-10 6 M-1) and cross-reactivity for anions, while the trans-isomer 1 shows a more selective response to anions. Such differences in binding mode in configurational isomers are so far unexplored and a feature deserving further study.

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