873854-89-8 Usage
Ester derivative
1H-Pyrrole-2-carboxylic acid, 3-formyl-1,4,5-trimethyl-, phenylmethyl ester is derived from pyrrole carboxylic acid and contains an ester functional group.
Contains a phenylmethyl group
The compound has a phenylmethyl (benzyl) group attached to the ester, which contributes to its aromatic properties.
Aromatic properties
The compound has aromatic characteristics due to the presence of the phenylmethyl group and the pyrrole ring.
Used in organic synthesis and pharmaceutical research
1H-Pyrrole-2-carboxylic acid, 3-formyl-1,4,5-trimethyl-, phenylmethyl ester is commonly used as a building block for synthesizing various compounds and in the development of new drugs and biologically active molecules.
Versatile building block
The compound can be used as a starting material for creating a wide range of chemical structures.
Potential therapeutic applications
The compound may have potential uses in the development of new drugs and treatments due to its unique structure and properties.
Possible use in materials science
1H-Pyrrole-2-carboxylic acid, 3-formyl-1,4,5-trimethyl-, phenylmethyl ester may be explored for its potential applications in the field of materials science, such as the development of new materials with unique properties.
Use as a dye or pigment
The compound may also have potential applications as a dye or pigment due to its aromatic and conjugated system, which can impart color to materials.
Check Digit Verification of cas no
The CAS Registry Mumber 873854-89-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,8,5 and 4 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 873854-89:
(8*8)+(7*7)+(6*3)+(5*8)+(4*5)+(3*4)+(2*8)+(1*9)=228
228 % 10 = 8
So 873854-89-8 is a valid CAS Registry Number.
873854-89-8Relevant academic research and scientific papers
Boiadjiev, Stefan E.,Lightner, David A.
, p. 553 - 565 (2005)
In "one-pot" reactions, pyrrole-α- and β-aldehydes condense readily with 4-ethyl-3-methyl-3-pyrrolin-2-one to give isodipyrrinone analogs, which undergo intramolecular cyclization when the pyrrolealdehyde possesses an α or β-CO2R group. The res
