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| Classification | Organic raw materials >> Ketone compound |
|---|---|
| Name | 5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehyde |
| Molecular Structure | ![]() |
| Molecular Formula | C11H8FNO |
| Molecular Weight | 189.19 |
| CAS Registry Number | 881674-56-2 |
| EC Number | 809-913-6 |
| SMILES | C1=CC=C(C(=C1)C2=CC(=CN2)C=O)F |
| Solubility | Very slightly soluble (0.13 g/L) (25 ºC), Calc.* |
|---|---|
| Density | 1.270±0.06 g/cm3 (20 ºC 760 Torr), Calc.* |
| * | Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2014 ACD/Labs) |
| Hazard Symbols |
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| Hazard Statements | H302-H312-H315-H319-H332-H335 Details | ||||||||||||||||||||||||||||||||
| Precautionary Statements | P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501 Details | ||||||||||||||||||||||||||||||||
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| SDS | Available | ||||||||||||||||||||||||||||||||
| 5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehyde is an organic compound discovered through medicinal chemistry research aiming to develop new molecules with potential pharmaceutical applications. The compound was first synthesized by reacting 2-fluorobenzaldehyde with pyrrole in a controlled environment, leading to the formation of the pyrrole carboxaldehyde derivative. The incorporation of a fluorine atom in the phenyl ring significantly influenced the compound's chemical properties, enhancing its potential for various biological activities. This discovery has paved the way for further exploration into the compound's applications, particularly in drug development and materials science. |
| Market Analysis Reports |
| List of Reports Available for 5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehyde |