82097-82-3

Basic information

• Product Name: 2-(2-fluorophenoxy)benzaldehyde
• Synonyms: 2-(2-fluorophenoxy)benzaldehyde
• CAS NO: 82097-82-3
• Molecular Formula: C₁₃H₉FO₂
• Molecular Weight: 216.2077632
• Mol File: 82097-82-3.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(2-fluorophenoxy)benzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-fluorophenoxy)benzaldehyde(82097-82-3)
• EPA Substance Registry System: 2-(2-fluorophenoxy)benzaldehyde(82097-82-3)

Safety Data

• Hazardous Substances Data: 82097-82-3(Hazardous Substances Data)

Usage

Benzaldehyde derivative

It is a derivative of benzaldehyde, which means it is a compound formed by the modification of the benzaldehyde structure.

Contains a fluorine atom

The compound has a fluorine atom in its structure, which can influence its chemical properties and reactivity.

Contains a phenoxy group

The presence of a phenoxy group (a phenol ether) in the structure contributes to its chemical properties and applications.

Used as an intermediate

2-(2-fluorophenoxy)benzaldehyde is commonly used as an intermediate in the synthesis of various organic compounds.

Potential applications

It has potential applications in the pharmaceutical and chemical industries, possibly due to its unique structure and reactivity.

Physical appearance

The compound is a white to light yellow solid with a characteristic aromatic odor.

Solubility

2-(2-fluorophenoxy)benzaldehyde is insoluble in water but soluble in organic solvents, which can affect its handling and use in chemical reactions.

Safety precautions

It is important to handle this chemical with care and follow proper safety precautions due to its potential hazards, such as irritation or toxicity.

Upstream product

• 367-12-4 2-fluorophenol 
• 446-52-6 2-Fluorobenzaldehyde 
• 2795-61-1 2-(2-fluoro-phenoxy)-benzoic acid 
• 321-28-8 1-fluoro-2-methoxybenzene 
• 81890-62-2 2-(2-fluorophenoxy)benzyl alcohol 

Downstream Products

• 329235-41-8 2'-fluoro-2-hydroxybenzophenone 
• 81890-63-3 1-<2-(2-fluorophenoxy)phenyl>-4-dimethylaminobutanol 

Relevant articles and documents

Discovery of Pyrazine-Carboxamide-Diphenyl-Ethers as Novel Succinate Dehydrogenase Inhibitors via Fragment Recombination

The discovery of novel succinate dehydrogenase inhibitors (SDHIs) has attracted great attention worldwide. Herein, a fragment recombination strategy was proposed to design new SDHIs by understanding the ligand-receptor interaction mechanism of SDHIs. Thre

Design, synthesis, and pharmacological evaluation of azetedine and pyrrolidine derivatives as dual norepinephrine reuptake inhibitors and 5-HT 1A partial agonists

Compounds with combined norepinephrine reuptake inhibitor (NRI) and serotonin 1A (5-HT1A) partial agonist pharmacology may offer a new therapeutic approach for treating symptoms of neuropsychiatric disorders including ADHD, depression, and anxiety. Herein we describe the design and optimization of novel chemical matter that exhibits favorable dual NRI and 5-HT1A partial agonist activity. Lead compounds in this series were found to be devoid of activity at the dopamine transporter and were shown to be brain penetrant with high receptor occupancy.

Tricyclic compounds

A technique is described for the preparation of a wide variety of basic derivatives of linearly condensed tricyclic systems formed by two external benzene nuclei and a 7-membered central ring having 2 chalcogen atoms as hetero atoms. Derivatives of 11H-dibenzo(b,e)-1,4-dioxepin are obtained when the chalcogens are both oxygen atoms; derivatives of 11H-dibenzo(b,f)-1,4-dithiepin are obtained when the chalcogens are both sulfur atoms; derivatives of 6H-dibenz(b,e)-1,4-oxathiepin and 11H-dibenz(b,f)-1,4-oxathiepin are obtained with combinations of sulfur and oxygen atoms as chalcogens.