52887-35-1 Usage
General Description
4-Benzyl 2-ethyl 3-(2-ethoxy-2-oxoethyl)-5-methyl-1H-pyrrole-2,4-dicarboxylate is a complex organic compound with a long molecular structure. It contains a benzyl group, an ethyl group, and a pyrrole ring, as well as two carboxylate groups. The compound also features an ethoxy-oxoethyl substituent. 4-BENZYL 2-ETHYL 3-(2-ETHOXY-2-OXOETHYL)-5-METHYL-1H-PYRROLE-2,4-DICARBOXYLATE has potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties. It may also have potential for use in the synthesis of novel drug molecules or as a building block in organic synthesis.
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 articles and documents
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.
