130274-66-7 Usage
Derivative of pyrrole
Pyrrole is a five-membered aromatic heterocycle The compound is based on the pyrrole structure, which consists of a five-membered ring with one nitrogen atom and four carbon atoms, known for its aromatic properties.
Five-membered ring
The pyrrole core has a five-membered structure The compound retains the five-membered ring characteristic of pyrrole, which contributes to its aromatic nature and stability.
Aromatic heterocycle
Pyrrole is an aromatic heterocycle The presence of the nitrogen atom in the five-membered ring gives the compound its aromatic properties, making it a desirable structure for various applications in organic synthesis and medicinal chemistry.
Two carboxaldehyde functional groups
The compound contains two aldehyde groups These functional groups are present at the 2 and 5 positions of the pyrrole ring, which can participate in various chemical reactions and contribute to the compound's reactivity.
Two ethyl substituents
The compound has two ethyl groups attached to the 3 and 4 positions These substituents are located on the pyrrole ring and can influence the compound's physical and chemical properties, as well as its reactivity.
Potential applications in organic synthesis
The compound's structural features and reactivity make it a candidate for use in organic synthesis Due to its unique structure and functional groups, 1H-Pyrrole-2,5-dicarboxaldehyde,3,4-diethyl-(9CI) can be used as a building block or intermediate in the synthesis of more complex organic molecules.
Potential applications in medicinal chemistry
The compound's structural features and reactivity may be useful in the development of new pharmaceuticals The presence of the pyrrole ring and various functional groups in the compound may contribute to its biological activity, making it a potential candidate for further investigation in medicinal chemistry.
Further research needed
More studies are required to explore the specific properties and potential uses of the compound in various fields Although 1H-Pyrrole-2,5-dicarboxaldehyde,3,4-diethyl-(9CI) shows promise in organic synthesis and medicinal chemistry, additional research is necessary to fully understand its properties and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 130274-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,2,7 and 4 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 130274-66:
(8*1)+(7*3)+(6*0)+(5*2)+(4*7)+(3*4)+(2*6)+(1*6)=97
97 % 10 = 7
So 130274-66-7 is a valid CAS Registry Number.
130274-66-7Relevant articles and documents
Intermolecularly hydrogen-bonded dimeric helices: tripyrrindiones
Roth, Steven D.,Shkindel, Tetyana,Lightner, David A.
, p. 11030 - 11039 (2007)
A rare and unusual class of tripyrrolic compounds, violet-colored tripyrrin-1,14-diones, can be prepared easily and in moderately high yields from base (piperidine)-catalyzed condensation of 3-pyrrolin-2-ones with 2,5-diformylpyrroles. Dipyrrinones adopt the all-syn-Z conformation leading to helical, lock-washer like structures, which form dimers that are held together by intermolecular hydrogen bonds in nonpolar solvents and in the crystal. Strong bathochromic spectral shifts of the tripyrrindione ～480 nm long wavelength UV-visible absorption band are seen with added base: DBU, 615 nm; TFA, 573 nm; and Zn(OAc)2, 586 nm.
New one-step synthesis of 3,4-disubstituted pyrrole-2,5-dicarbaldehydes
Tardieux, Catherine,Bolze, Frederic,Gros, Claude P.,Guilard, Roger
, p. 267 - 268 (1998)
A smooth and convenient one-step synthesis of 3,4-disubstituted pyrrole- 2,5-dicarbaldehydes 2 is reported. This reaction involves the condensation of β-substituted pyrrole-2-carboxylic acids with triethyl orthoformate in trifluoroacetic acid to give the title compounds in good yield.
Die Porphyrin-Homologen: Porphyrin(2.2.2.2), ein "gestrecktes Porphycen"
Vogel, Emanuel,Jux, Norbert,Rodriguez-Val, Eduardo,Lex, Johann,Schmickler, Hans
, p. 1431 - 1434 (2007/10/02)
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