5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehyde
[CAS# 881674-56-2]

Identification

• Classification: Organic raw materials >> Ketone compound
• Name: 5-(2-Fluorophenyl)-1H-pyrrole-3-carboxaldehyde
• 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

Properties

• Solubility: Very slightly soluble (0.13 g/L) (25 °C), Calc.^*
• Density: 1.270±0.06 g/cm³ (20 °C 760 Torr), Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2014 ACD/Labs)

Safety Data

• Hazard Symbols: GHS07 Warning
• Risk Statements: H302-H312-H315-H319-H332-H335
• Safety 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

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Acute toxicity	Acute Tox.	4	H332
Specific target organ toxicity - single exposure	STOT SE	3	H335
Acute toxicity	Acute Tox.	4	H302
Acute toxicity	Acute Tox.	4	H312
Eye irritation	Eye Irrit.	2A	H319
Skin irritation	Skin Irrit.	2	H315

Discovery and Applications

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.

References

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