280576-52-5 Usage
Molecular structure
1H-Pyrrole-3-carboxaldehyde, 5-methoxy-1-(4-methoxyphenyl)-2-(methyl-2-propenylamino)contains a pyrrole ring, a carboxaldehyde group, a methoxy group, a phenyl group, and a methyl-2-propenylamino group.
Functional groups
The compound has a carboxaldehyde group (-CHO) attached at position 3, a methoxy group (-OCH3) at position 5, a methoxy group (-OCH3) attached to the phenyl group at position 4, and a methyl-2-propenylamino group (-NH-CH=C(CH3)2) attached at position 2.
Aromatic systems
The compound contains a pyrrole ring and a phenyl ring, both of which are aromatic systems.
Substitution patterns
The compound has a methoxy group at position 5 of the pyrrole ring, a methoxy group at position 4 of the phenyl ring, and a methyl-2-propenylamino group at position 2 of the pyrrole ring.
Potential applications
1H-Pyrrole-3-carboxaldehyde, 5-methoxy-1-(4-methoxyphenyl)-2-(methyl-2-propenylamino)has potential applications in pharmaceuticals, agrochemicals, and materials science.
Biological activities
The compound has unique structural features and potential biological activities that require further research and development to fully understand its properties and potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 280576-52-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,0,5,7 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 280576-52:
(8*2)+(7*8)+(6*0)+(5*5)+(4*7)+(3*6)+(2*5)+(1*2)=155
155 % 10 = 5
So 280576-52-5 is a valid CAS Registry Number.
280576-52-5Relevant academic research and scientific papers
1-Aryl-2-chloro-5-methoxy-1H-3-pyrrolecarbaldehyde as synthons for fused heterocycles: synthesis of pyrazolo[3,4-d]pyrrolo[2,3-b]pyridine derivatives
El-Nabi, Hisham A. Abd
, p. 325 - 327 (2007/10/03)
Pyrazolo[3,4-d]pyrrolo[2,3-b]pyridine derivatives (6a-f) were obtained by oxidation of tosylhydrazones of 2-allylamino-5-methoxypyrrole-3-carbaldehydes (3a-f) with lead tetraacetate. The nitrilimine intermediates (5a-f) underwent intramolecular 1,3-dipolar cycloaddition to yield the tricyclic heterocycles 6a-f in good yields.
1-Aryl-5-methoxy-pyrrolones as synthons for 1,3-dipolar cycloadditions
Abd El-Nabi, Hisham A.
, p. 3013 - 3020 (2007/10/03)
A general method is described to convert the title compound into more complex nitrogen heterocyclic systems in a short and attractive pathway. Spiroisoxazolidine 6 was obtained from the reaction of nitrone 3 with ethyl vinyl ether. Chloroformylation of pyrrolone 2 gave 1-aryl-2-chloro-5-methoxy- pyrrol-3-carbaldehyde 4. Substitution of chlorine atom with unsaturated nucleophiles 8a,b and then modifying the aldehyde function into 1,3-dipoles 10 and 14 furnished tricyclic heterocycles 11, 12 and 15 via intramolecular 1,3-dipolar cycloaddition reaction. (C) 2000 Elsevier Science Ltd.
