548740-24-5 Usage
Description
(Z)-methyl3-(2,4-dimethyl-5-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoate is a complex organic chemical compound characterized by its unique molecular structure. It features a methyl group attached to a carbon chain, which is connected to a pyrrole ring that contains both a dimethyl and a (2-oxoindolin-3-ylidene)methyl group. (Z)-methyl3-(2,4-dimethyl-5-((2-oxoindolin3-ylidene)methyl)-1H-pyrrol-3-yl)propanoate is known for its potential applications in various scientific fields due to its distinctive structural and reactivity properties.
Uses
Used in Research and Development:
(Z)-methyl3-(2,4-dimethyl-5-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoate is utilized as a building block in the synthesis of other organic compounds, making it a valuable asset for research and development in the field of chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (Z)-methyl3-(2,4-dimethyl-5-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoate is used as a key intermediate for the development of new drugs. Its unique structure and reactivity contribute to the creation of novel pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
(Z)-methyl3-(2,4-dimethyl-5-((2-oxoindolin-3-ylidene)methyl)-1H-pyrrol-3-yl)propanoate also holds promise in the agrochemical industry, where it may be employed as a starting material for the synthesis of new agrochemicals, such as pesticides or herbicides, that could improve agricultural productivity and crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 548740-24-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,7,4 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 548740-24:
(8*5)+(7*4)+(6*8)+(5*7)+(4*4)+(3*0)+(2*2)+(1*4)=175
175 % 10 = 5
So 548740-24-5 is a valid CAS Registry Number.
548740-24-5Relevant articles and documents
Syntheses and properties of benzodipyrrinones
Boiadjiev, Stefan E.,Lightner, David A.
, p. 181 - 185 (2003)
2,3-Benzannelated dipyrrinone analogs (1 and 2) of xanthobilirubic acid (3) are prepared by base-catalyzed condensation of isoindolinone (5) and indolin-2-one (6) respectively, with methyl 3-(2-formyl-3,5-dimethyl-1H-pyrrol-4-yl)propanoate (4). Nuclear Overhauser effect H-nmr studies indicate that both 1 and 2 adopt preferentially a syn-Z configuration. The former forms a hydrogen-bonded homodimer in nonpolar solvents; the latter is intramolecularly hydrogen bonded.
