128843-61-8 Usage
General Description
4-(4-Fluorobenzoyl)-1-Methyl-1H-Pyrrole-2-Carbaldehyde is a complex organic chemical compound. This substance is characterized by a combination of fluorine, a pyrrole ring, a methyl group, and a carbonyl group, which includes a fluorobenzoyl group and an aldehyde group. Additionally, its 1-methyl-1H-pyrrole-2-carbaldehyde refers to a heterocyclic aromatic compound that forms an essential part of many important biomolecules and it also contains a benzene ring in its structure, which contributes to its stability and resonance. Typically, these type of compounds are used in various fields, including the pharmaceutical industry, chemical research, and other industrial applications. However, specific details about its usage, properties, and potential health and environmental impacts are not widely documented and would require further specific research.
Check Digit Verification of cas no
The CAS Registry Mumber 128843-61-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,4 and 3 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128843-61:
(8*1)+(7*2)+(6*8)+(5*8)+(4*4)+(3*3)+(2*6)+(1*1)=148
148 % 10 = 8
So 128843-61-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H10FNO2/c1-15-7-10(6-12(15)8-16)13(17)9-2-4-11(14)5-3-9/h2-8H,1H3
128843-61-8Relevant articles and documents
Structure-activity relationship of pyrrolyl diketo acid derivatives as dual inhibitors of HIV-1 integrase and reverse transcriptase ribonuclease H domain
Cuzzucoli Crucitti, Giuliana,Métifiot, Mathieu,Pescatori, Luca,Messore, Antonella,Madia, Valentina Noemi,Pupo, Giovanni,Saccoliti, Francesco,Scipione, Luigi,Tortorella, Silvano,Esposito, Francesca,Corona, Angela,Cadeddu, Marta,Marchand, Christophe,Pommier, Yves,Tramontano, Enzo,Costi, Roberta,Di Santo, Roberto
, p. 1915 - 1928 (2015/04/27)
The development of HIV-1 dual inhibitors is a highly innovative approach aimed at reducing drug toxic side effects as well as therapeutic costs. HIV-1 integrase (IN) and reverse transcriptase-associated ribonuclease H (RNase H) are both selective targets
3-(4-Aroyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides, a new class of synthetic histone deacetylase inhibitors
Massa,Mai,Sbardella,Esposito,Ragno,Loidl,Brosch
, p. 2069 - 2072 (2007/10/03)
Novel 3-(4-aroyl-2-pyrrolyl)-N-hydroxy-2-propenamides are disclosed as a new class of histone deacetylase (HDAC) inhibitors. Three-dimensional structure-based drug design and conformational analyses into the histone deacetylase-like protein (HDLP) catalyt