52887-35-1 Usage
Uses
Used in Pharmaceutical Industry:
4-Benzyl 2-ethyl 3-(2-ethoxy-2-oxoethyl)-5-methyl-1H-pyrrole-2,4-dicarboxylate is used as a key intermediate in the synthesis of novel drug molecules, leveraging its unique structure to contribute to the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Benzyl 2-ethyl 3-(2-ethoxy-2-oxoethyl)-5-methyl-1H-pyrrole-2,4-dicarboxylate is used as a component in the formulation of new agrochemical products, potentially enhancing the effectiveness of pesticides or other agricultural chemicals.
Used in Materials Science:
4-Benzyl 2-ethyl 3-(2-ethoxy-2-oxoethyl)-5-methyl-1H-pyrrole-2,4-dicarboxylate is utilized in materials science for the development of new materials with specific properties, such as improved stability or reactivity, due to its unique molecular composition.
Used in Organic Synthesis:
As a building block in organic synthesis, 4-Benzyl 2-ethyl 3-(2-ethoxy-2-oxoethyl)-5-methyl-1H-pyrrole-2,4-dicarboxylate is employed to construct more complex organic molecules, contributing to the advancement of organic chemistry and the creation of new compounds with various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 52887-35-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,8,8 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52887-35:
(7*5)+(6*2)+(5*8)+(4*8)+(3*7)+(2*3)+(1*5)=151
151 % 10 = 1
So 52887-35-1 is a valid CAS Registry Number.
InChI:InChI=1/C20H23NO6/c1-4-25-16(22)11-15-17(13(3)21-18(15)20(24)26-5-2)19(23)27-12-14-9-7-6-8-10-14/h6-10,21H,4-5,11-12H2,1-3H3
52887-35-1Relevant academic research and scientific papers
Chemically reactive dipyrrometheneboron difluoride dyes
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, (2008/06/13)
Novel fluorescent dyes based on the dipyrrometheneboron difluoride structure are provided. The new reagents contain functional groups capable of forming a stable fluorescent product with functional groups typically found in biomolecules or polymers including amines, phenols, thiols, acids, aldehydes and ketones. Reactive groups in the dipyrrometheneboron difluoride dyes include activated esters, isocyanates, amines, hydrazines, sulfonyl halides, acids, aldehydes, alcohols and haloacetamides. The products are detected by their absorbance or fluorescence properties. The spectral properties of the fluorescent dyes are sufficiently similar in wavelengths and intensity to fluorescein as to permit use of the same euqipment. The dyes, however, have narrower spectral bandwidths than fluorescein, do not show appreciable sensitivity to pH, have higher solubility in non-polar solvents and have improved photostability.
