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Catalog Number:
45186
CAS Number:
68359-57-9
4-Fluoro-3-phenoxybenzaldehyde
Purity:
≥ 97% (GC)
Synonym(s):
2-Fluoro-5-formyldiphenyl Ether
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Product Information

4-Fluoro-3-phenoxybenzaldehyde is a versatile aromatic compound that plays a significant role in various chemical syntheses and applications. This compound is recognized for its unique fluorine substitution, which enhances its reactivity and stability, making it an ideal candidate for use in the development of pharmaceuticals and agrochemicals. Its phenoxy group contributes to its solubility and compatibility with a range of organic solvents, facilitating its use in diverse chemical reactions. Researchers and industry professionals often utilize 4-Fluoro-3-phenoxybenzaldehyde in the synthesis of complex organic molecules, including biologically active compounds and intermediates in drug discovery.

In addition to its synthetic applications, this compound is also valuable in the formulation of specialty chemicals and materials. Its distinctive properties enable it to act as a key building block in the production of dyes, fragrances, and other fine chemicals. The ability to modify its structure further enhances its utility, allowing for tailored applications in various sectors. With its combination of reactivity and functional versatility, 4-Fluoro-3-phenoxybenzaldehyde stands out as a crucial component for researchers and manufacturers looking to innovate and expand their product offerings.

Synonyms
2-Fluoro-5-formyldiphenyl Ether
CAS Number
68359-57-9
Purity
≥ 97% (GC)
Molecular Formula
C13H9FO2
Molecular Weight
216.21
MDL Number
MFCD01318148
PubChem ID
110068
Density
1.23
Appearance
Colorless to light orange to yellow clear liquid
Boiling Point
135 °C/2 mmHg
Refractive Index
n20D 1.58
Conditions
Store at RT
General Information
Synonyms
2-Fluoro-5-formyldiphenyl Ether
CAS Number
68359-57-9
Purity
≥ 97% (GC)
Molecular Formula
C13H9FO2
Molecular Weight
216.21
MDL Number
MFCD01318148
PubChem ID
110068
Density
1.23
Appearance
Colorless to light orange to yellow clear liquid
Boiling Point
135 °C/2 mmHg
Refractive Index
n20D 1.58
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Fluoro-3-phenoxybenzaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs. Its unique structure allows for targeted modifications that enhance therapeutic efficacy.
  • Agricultural Chemicals: It is used in the formulation of agrochemicals, including herbicides and insecticides. The compound's properties help improve the effectiveness of these products, leading to better crop yields and pest management.
  • Material Science: In the production of specialty polymers, this chemical acts as a building block for creating materials with enhanced thermal and chemical resistance, making it valuable in industries such as automotive and aerospace.
  • Organic Synthesis: Researchers utilize it in various organic synthesis reactions, including coupling reactions, due to its reactivity and ability to form stable intermediates. This makes it a versatile tool in synthetic chemistry.
  • Analytical Chemistry: It is employed as a standard in analytical methods, helping to calibrate instruments and validate results in laboratories, ensuring accuracy in chemical analysis.

Citations