19406-11-2 Usage
Uses
1H-Pyrrole-3-carboxylic acid, 1,2-dimethyl-, ethyl ester is used as a chemical intermediate for the synthesis of various organic compounds. Its unique molecular structure, including the pyrrole ring and the ethyl ester group, may provide it with specific reactivity that can be exploited in the preparation of pharmaceuticals, agrochemicals, or other specialty chemicals.
Used in Pharmaceutical Industry:
1H-Pyrrole-3-carboxylic acid, 1,2-dimethyl-, ethyl ester is used as a building block in the development of new drugs. Its chemical properties may allow it to form key structural elements in drug molecules, potentially leading to the discovery of novel therapeutic agents.
Used in Agrochemical Industry:
1H-Pyrrole-3-carboxylic acid, 1,2-dimethyl-, ethyl ester is used as a precursor in the synthesis of agrochemicals. Its potential reactivity and solubility characteristics could be harnessed to create new compounds with pesticidal or herbicidal properties.
Used in Specialty Chemicals Industry:
1H-Pyrrole-3-carboxylic acid, 1,2-dimethyl-, ethyl ester is used as a component in the formulation of specialty chemicals. Its unique structure may contribute to the development of new materials with specific properties, such as dyes, pigments, or polymers with tailored characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 19406-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,0 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19406-11:
(7*1)+(6*9)+(5*4)+(4*0)+(3*6)+(2*1)+(1*1)=102
102 % 10 = 2
So 19406-11-2 is a valid CAS Registry Number.
19406-11-2Relevant academic research and scientific papers
Reactions of Carbethoxycarbene with Enaminones. Formation of Unexpected Pyrroles
Augusti, Rodinei,Eberlin, Marcos N.,Kascheres, Concetta
, p. 1355 - 1358 (2007/10/03)
The reactions of carbethoxycarbene (:CH2-CO2Et, 2) with several acyclic enaminones (RCOCH=CR1NHR2, 3) lead to the unexpected formation of 2-Me, 3-CO2Et, 4-H, 5-R1-pyrroles 4.Structural variations of the enaminones show that the structural fragments C(3)-CO2Et and C(2)-Me are provided by 2 and that the fragment C(5)-R1NHR2 originates from the enaminones 3, while the RCO group from 3 is eliminated during the course of reaction.Reactions with cyclic and nitrogen-hindered enaminones do not lead to pyrrole formation but occur by simple insertion of 2 to the Cα-H bond.
