1-(3-fluorophenyl)-N-((3-fluorophenyl)methylideneamino)methanimine
Overview[edit | edit source]
1-(3-fluorophenyl)-N-((3-fluorophenyl)methylideneamino)methanimine is a chemical compound that belongs to the class of Schiff bases. Schiff bases are characterized by the presence of a functional group that contains a carbon-nitrogen double bond with the nitrogen atom connected to an aryl or alkyl group, but not hydrogen. This compound is of interest in the field of organic chemistry and has potential applications in various chemical reactions and processes.
Chemical Structure[edit | edit source]
The chemical structure of 1-(3-fluorophenyl)-N-((3-fluorophenyl)methylideneamino)methanimine can be described by the following features:
- Molecular Formula: C13H9F2N
- Molecular Weight: 217.22 g/mol
- Functional Groups: The compound contains two 3-fluorophenyl groups and a Schiff base linkage.
The structure can be represented as:
```
F |
C6H4-CH=N-C6H4-F ```
Synthesis[edit | edit source]
The synthesis of 1-(3-fluorophenyl)-N-((3-fluorophenyl)methylideneamino)methanimine typically involves the condensation reaction between an amine and an aldehyde or ketone. In this case, the reaction involves the condensation of 3-fluorobenzaldehyde with 3-fluoroaniline. The reaction is usually carried out in a solvent such as ethanol or methanol, and may require a catalyst or acidic conditions to proceed efficiently.
Applications[edit | edit source]
Schiff bases, including 1-(3-fluorophenyl)-N-((3-fluorophenyl)methylideneamino)methanimine, are used in various applications:
- Catalysis: Schiff bases can act as ligands in coordination chemistry, forming complexes with metals that can be used as catalysts in organic reactions.
- Biological Activity: Some Schiff bases have been studied for their potential biological activities, including antimicrobial, antifungal, and anticancer properties.
- Material Science: Schiff bases can be used in the synthesis of polymers and other materials with specific properties.
Safety and Handling[edit | edit source]
As with many chemical compounds, proper safety precautions should be taken when handling 1-(3-fluorophenyl)-N-((3-fluorophenyl)methylideneamino)methanimine. This includes wearing appropriate personal protective equipment (PPE) such as gloves and goggles, and working in a well-ventilated area or fume hood.
Also see[edit | edit source]
Search WikiMD
Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD
WikiMD's Wellness Encyclopedia |
Let Food Be Thy Medicine Medicine Thy Food - Hippocrates |
Translate this page: - East Asian
中文,
日本,
한국어,
South Asian
हिन्दी,
தமிழ்,
తెలుగు,
Urdu,
ಕನ್ನಡ,
Southeast Asian
Indonesian,
Vietnamese,
Thai,
မြန်မာဘာသာ,
বাংলা
European
español,
Deutsch,
français,
Greek,
português do Brasil,
polski,
română,
русский,
Nederlands,
norsk,
svenska,
suomi,
Italian
Middle Eastern & African
عربى,
Turkish,
Persian,
Hebrew,
Afrikaans,
isiZulu,
Kiswahili,
Other
Bulgarian,
Hungarian,
Czech,
Swedish,
മലയാളം,
मराठी,
ਪੰਜਾਬੀ,
ગુજરાતી,
Portuguese,
Ukrainian
Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.
Contributors: Prab R. Tumpati, MD