40565-85-3 Usage
Ethyl ester of 4-formyl-5-iodo-1H-pyrrole-2-carboxylic acid
1H-Pyrrole-2-carboxylic acid, 4-formyl-5-iodo-, ethyl ester is an ethyl ester, meaning it has an ethoxy group (OC2H5) attached to the carboxylic acid (COOH) functional group of 4-formyl-5-iodo-1H-pyrrole-2-carboxylic acid.
Used in organic synthesis and medicinal chemistry
1H-Pyrrole-2-carboxylic acid, 4-formyl-5-iodo-, ethyl ester is commonly used as a building block in the synthesis of bioactive molecules, making it a valuable reagent in the development of novel compounds for drug discovery and chemical research.
Potential pharmaceutical applications
Due to its unique structure and iodine substituent, 1H-Pyrrole-2-carboxylic acid, 4-formyl-5-iodo-, ethyl ester has potential applications in the pharmaceutical industry as a building block for the synthesis of bioactive molecules.
Valuable reagent
The unique structure and iodine substituent of 1H-Pyrrole-2-carboxylic acid, 4-formyl-5-iodo-, ethyl ester make it a valuable reagent in the development of novel compounds for drug discovery and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 40565-85-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,6 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 40565-85:
(7*4)+(6*0)+(5*5)+(4*6)+(3*5)+(2*8)+(1*5)=113
113 % 10 = 3
So 40565-85-3 is a valid CAS Registry Number.
40565-85-3Relevant academic research and scientific papers
Synthesis of new tetracyclic paullone derivatives as potential CDK inhibitors
Koutsandrea, Efthimia G.,Fousteris, Manolis A.,Nikolaropoulos, Sotiris S.
, p. 169 - 179 (2013/01/16)
Synthetic efforts towards new tetracyclic heterocycles bearing the pyrrolo[2',3':5,6]azepino[4,3- b ] indol-4(11 H )-one core are described. Synthesized tetracyclic compounds are the first analogs, structurally related to protein kinase inhibitors paullones which incorporate an azepinone, an indole and a pyrrole ring. The synthetic approach involves palladium mediated intramolecular Heck coupling as a key step.
