Cas no 69888-91-1 (3-(3-fluoro-4-hydroxyphenyl)propanoic acid)

3-(3-fluoro-4-hydroxyphenyl)propanoic acid structure
69888-91-1 structure
Product Name:3-(3-fluoro-4-hydroxyphenyl)propanoic acid
CAS No:69888-91-1
MF:C9H9FO3
MW:184.164366483688
CID:517423
PubChem ID:3017967
Update Time:2025-04-23

3-(3-fluoro-4-hydroxyphenyl)propanoic acid Chemical and Physical Properties

Names and Identifiers

    • Benzenepropanoic acid,3-fluoro-4-hydroxy-
    • 3-(3-fluoro-4-hydroxyphenyl)propanoic acid
    • 3-(3-fluoro-4-hydroxyphenyl)propionic acid
    • NS00063128
    • 3-(3-fluoro-4-hydroxyphenyl)propanoicacid
    • 69888-91-1
    • EN300-1858359
    • DTXSID70990166
    • MFCD18396901
    • F52917
    • SCHEMBL3336184
    • A1-37796
    • RMXXLSLLEBZFBS-UHFFFAOYSA-N
    • EINECS 274-187-4
    • Inchi: 1S/C9H9FO3/c10-7-5-6(1-3-8(7)11)2-4-9(12)13/h1,3,5,11H,2,4H2,(H,12,13)
    • InChI Key: RMXXLSLLEBZFBS-UHFFFAOYSA-N
    • SMILES: FC1=C(C=CC(=C1)CCC(=O)O)O

Computed Properties

  • Exact Mass: 184.05357
  • Monoisotopic Mass: 184.053572
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 184
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 57.5
  • XLogP3: 1.4

Experimental Properties

  • Density: 1.353
  • Boiling Point: 329.3°C at 760 mmHg
  • Flash Point: 152.9°C
  • Refractive Index: 1.558
  • PSA: 57.53

3-(3-fluoro-4-hydroxyphenyl)propanoic acid Pricemore >>

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3-(3-fluoro-4-hydroxyphenyl)propanoic acid Related Literature

Additional information on 3-(3-fluoro-4-hydroxyphenyl)propanoic acid

Benzenepropanoic Acid, 3-Fluoro-4-Hydroxy (CAS No: 69888-91-1)

Benzenepropanoic acid, 3-fluoro-4-hydroxy, also known by its CAS registry number 69888-91-1, is a compound of significant interest in the fields of organic chemistry and pharmacology. This compound is characterized by its unique structure, which includes a benzenepropanoic acid backbone with specific substituents at the 3 and 4 positions of the benzene ring. The presence of a fluoro group at the 3 position and a hydroxy group at the 4 position imparts distinct chemical and biological properties to this molecule.

The synthesis of 3-fluoro-4-hydroxybenzenepropanoic acid involves a series of carefully controlled reactions, often starting from fluorobenzene derivatives. The introduction of the hydroxyl group typically requires precise oxidation or substitution reactions, ensuring minimal side reactions and high purity of the final product. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses, reducing production costs and minimizing waste.

One of the most notable applications of this compound is in the development of novel pharmaceutical agents. Researchers have explored its potential as a precursor for bioactive molecules, particularly in the areas of anti-inflammatory and antioxidant therapies. Studies published in reputable journals such as Journal of Medicinal Chemistry have highlighted its ability to modulate key cellular pathways involved in inflammation and oxidative stress.

In addition to its pharmacological applications, 3-fluoro-4-hydroxybenzenepropanoic acid has shown promise in materials science. Its unique electronic properties make it a candidate for use in organic semiconductors and advanced polymers. Recent research has focused on optimizing its integration into polymer systems to enhance mechanical stability and electrical conductivity.

The chemical stability of this compound is another area of active investigation. Under standard storage conditions, it exhibits excellent stability, making it suitable for long-term use in various industrial applications. However, exposure to certain environmental factors, such as UV light or high humidity, can lead to degradation. Advanced stabilization techniques are being developed to address these challenges.

In conclusion, Benzenepropanoic acid, 3-fluoro-4-hydroxy (CAS No: 69888-91-1) is a versatile compound with a wide range of potential applications across multiple disciplines. Its unique structure and properties continue to attract the attention of researchers worldwide, driving innovation and discovery in both academic and industrial settings.

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