161560-66-3 Usage
Molecular Weight
199.24 g/mol This is the mass of one mole of 1H-Pyrrole-3-carboxaldehyde, 5-benzoyl-1-methyl-, which is approximately 199.24 grams.
Chemical Class
Pyrrole Derivatives This indicates that 1H-Pyrrole-3-carboxaldehyde, 5-benzoyl-1-methylbelongs to a class of chemical compounds known as pyrrole derivatives, which are characterized by a five-membered ring structure with one nitrogen atom.
Usage in Synthesis
Organic Compounds and Pharmaceuticals This indicates that 1H-Pyrrole-3-carboxaldehyde, 5-benzoyl-1-methylis commonly used as a building block or intermediate in the synthesis of other organic compounds and pharmaceuticals due to its versatile and unique chemical properties.
Potential Applications
Therapeutic Drugs This suggests that 1H-Pyrrole-3-carboxaldehyde, 5-benzoyl-1-methylhas potential applications in the pharmaceutical industry, specifically in the development of new drugs with therapeutic properties.
Use as a Reagent
Chemical Reactions This indicates that 1H-Pyrrole-3-carboxaldehyde, 5-benzoyl-1-methylis used as a reagent in various chemical reactions, making it a valuable and important compound in organic chemistry research and manufacturing processes.
Check Digit Verification of cas no
The CAS Registry Mumber 161560-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,5,6 and 0 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161560-66:
(8*1)+(7*6)+(6*1)+(5*5)+(4*6)+(3*0)+(2*6)+(1*6)=123
123 % 10 = 3
So 161560-66-3 is a valid CAS Registry Number.
161560-66-3Relevant academic research and scientific papers
3-(4-Aroyl-1-methyl-1H-pyrrol-2-yl)-N-hydroxy-2-propenamides as a New Class of Synthetic Histone Deacetylase Inhibitors. 3. Discovery of Novel Lead Compounds through Structure-Based Drug Design and Docking Studies
Ragno, Rino,Mai, Antonello,Massa, Silvio,Cerbara, Ilaria,Valente, Sergio,Bottoni, Patrizia,Scatena, Roberto,Jesacher, Florian,Loidl, Peter,Brosch, Gerald
, p. 1351 - 1359 (2007/10/03)
Aroyl-pyrrole-hydroxy-amides (APHAs) are a new class of synthetic HDAC inhibitors recently described by us. Through three different docking procedures we designed, synthesized, and tested two new isomers of APHA lead compound 3-(4-benzoyl-1-methyl-1H-pyrr
Structure-Activity Relationships of (4-Acylpyrrol-2-yl)alkanoic Acids as Inhibitors of the Cytosolic Phospholipase A2: Variation of the Substituents in Positions 1, 3, and 5
Lehr, Matthias
, p. 3381 - 3392 (2007/10/03)
Derivatives of 3-(l,3,5-trimethyl-4-octadecanoylpyrrol-2-yl)propionic acid (1) and (1,3,5-trimethyl-4-octadecanoylpyrrol-2-yl)acetic acid (4) were prepared and evaluated for their ability to inhibit the cytosolic phospholipase A2 of intact bovine platelet
