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1H-Pyrrole-3-carboxylic acid, 2,5-dimethyl-4-(2-pyridinyl)-, ethyl ester is a complex organic compound with the chemical formula C14H16N2O2. It is a derivative of pyrrole-3-carboxylic acid, featuring a 2,5-dimethyl-4-(2-pyridinyl) substitution pattern. The ethyl ester group is attached to the carboxylic acid moiety, which influences its reactivity and solubility. 1H-Pyrrole-3-carboxylic acid, 2,5-dimethyl-4-(2-pyridinyl)-, ethyl ester is characterized by its unique molecular structure, which includes a pyrrole ring with two methyl groups at positions 2 and 5, and a pyridine ring attached at position 4. The ethyl ester functional group at the 3-position further modifies its chemical properties. Such compounds are often studied for their potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis due to their diverse reactivity and the ability to form complex molecular frameworks.

95838-63-4

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95838-63-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95838-63-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,3 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 95838-63:
(7*9)+(6*5)+(5*8)+(4*3)+(3*8)+(2*6)+(1*3)=184
184 % 10 = 4
So 95838-63-4 is a valid CAS Registry Number.

95838-63-4Downstream Products

95838-63-4Relevant academic research and scientific papers

Heterocycles from α-Nitroolefins, VIII. - 2-Methyl-3-pyrrolecarboxylates from α-Nitroolefins and Acetoacetates

Boberg, Friedrich,Garburg, Karl-Heinz,Goerlich, Karl-Joachim,Pipereit, Eberhard,Ruhr, Maria

, p. 239 - 250 (2007/10/02)

3-Pyrrolecarboxylates 4 can be prepared from α-nitroolefins 1 and acetoacetates 2 by two methods: (a) 1 and 2 react to give 4,5-dihydro-5-methyleneamino-3-furancarboxylates 3 which are hydrolyzed, (b) the nitronic acids 8, adducts of 1 and 2, yield with different reduction agents the heterocycles 4.

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