1579-78-8

Basic information

• Product Name: 3-(4-Fluorophenoxy)propionic acid
• Synonyms: 3-(4-FLUOROPHENOXY)PROPANOIC ACID;3-(4'-FLUOROPHENOXY)PROPIONIC ACID;3-(4-FLUOROPHENOXY)PROPIONIC ACID;BUTTPARK 21\07-85;IFLAB-BB F1924-0040;RARECHEM AL BO 1453;3-(4-Fluorophenoxy)propionic acid 97%;3-(4-Fluorophenoxy)propionicacid97%
• CAS NO: 1579-78-8
• Molecular Formula: C₉H₉FO₃
• Molecular Weight: 184.16
• EINECS: 216-424-6
• Product Categories: Aliphatics;Carboxylic Acids;Carboxylic Acids;C9;Carbonyl Compounds
• Mol File: 1579-78-8.mol
• Article Data: 7

Chemical Properties

• Melting Point: 83-85 °C(lit.)
• Boiling Point: 287.7 °C at 760 mmHg
• Flash Point: 127.8 °C
• Appearance: /
• Density: 1.267 g/cm³
• PKA: 4.82±0.10(Predicted)
• CAS DataBase Reference: 3-(4-Fluorophenoxy)propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-Fluorophenoxy)propionic acid(1579-78-8)
• EPA Substance Registry System: 3-(4-Fluorophenoxy)propionic acid(1579-78-8)

Safety Data

• Hazard Codes: C,Xi
• Statements: 36/37/38
• Safety Statements: 26-26
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 1579-78-8(Hazardous Substances Data)

Usage

Description

3-(4-Fluorophenoxy)propionic acid is an organic compound that can be synthesized using 3-(4-fluorophenoxy)propanenitrile as a starting reagent. It is characterized by the presence of a fluorophenoxy group attached to a propionic acid backbone, which may contribute to its potential applications in various industries.

Uses

Used in Pharmaceutical Industry:
3-(4-Fluorophenoxy)propionic acid is used as a reactant for the synthesis of 2,3-dihydro-6-fluoro-4H-1-benzopyran-4-one, which may have potential applications in the development of pharmaceutical compounds. The synthesis of such compounds could lead to the creation of new drugs with various therapeutic properties.
Used in Chemical Synthesis:
In the field of chemical synthesis, 3-(4-Fluorophenoxy)propionic acid serves as a valuable building block for the creation of more complex molecules. Its unique structure, which includes a fluorine atom and a phenoxy group, may impart specific reactivity or selectivity in chemical reactions, making it a useful component in the synthesis of a wide range of compounds.
Used in Research and Development:
3-(4-Fluorophenoxy)propionic acid may also be utilized in research and development settings, where it can be explored for its potential applications in various fields. Scientists and researchers can use this compound to study its properties, reactivity, and potential interactions with other molecules, which could lead to the discovery of new applications and uses.

Upstream product

• 107-94-8 chloropropionic acid 
• 371-41-5 4-Fluorophenol 
• 85169-02-4 3-(4-fluoro-phenoxy)propionitrile 
• 371-40-4 4-fluoroaniline 
• 590-92-1 3-Bromopropionic acid 
• 104413-57-2 3-(4-fluorophenoxy)-1-propanol 

Downstream Products

• 66892-34-0 6-fluoro-4-chromanone 
• 81098-60-4 Acenalin 
• 368424-43-5 1-[3-(4-fluoro-phenoxy)-propionyl]-3-methoxy-piperidin-4-one 
• 368424-42-4 3-(4-fluoro-phenoxy)-1-(3,4,4-trimethoxy-piperidin-1-yl)-propan-1-one 
• 368424-41-3 3-(4-fluoro-phenoxy)-1-(3-hydroxy-4,4-dimethoxy-piperidin-1-yl)-propan-1-one 
• 69684-83-9 (+/-)-sorbinil 
• 67146-05-8 sorbinil 
• 104413-57-2 3-(4-fluorophenoxy)-1-propanol 
• 1093091-71-4 2-(4-{3-[(4-fluorophenyl)oxy]propanoyl}-1-piperazinyl)-6-(trifluoromethyl)benzonitrile 
• 1093092-10-4 1,1-dimethylethyl 4-{3-[(4-fluorophenyl)oxy]propanoyl}-1-piperazine carboxylate 
• 1093091-95-2 2-(4-{3-[(4-Fluorophenyl)oxy]propanoyl}-1-piperazinyl)benzonitrile 
• 1245316-32-8 N-(2-amino-4,6-dihydroxypyrimidin-5-yl)-3-(4-fluorophenoxy)propanamide 
• 1245316-55-5 5-amino-2-(2-(4-fluorophenoxy)ethyl)-thiazolo[5,4-d]pyrimidine-7-thiol 
• 1245316-54-4 2-(2-(4-fluorophenoxy)ethyl)-7-(methylthio)thiazolo[5,4-d]-pyrimidin-5-amine 

Relevant articles and documents

Acid activated montmorillonite K-10 mediated intramolecular acylation: Simple and convenient synthesis of 4-chromanones

3-Aryloxyproionic acids undergo intramolecular cyclization in the presence of AA.Mont.K-10 in toluene under reflux for 30–45 min in good to excellent yields. Phenyl ring bearing various substituents at the ortho, meta, para positions undergo this cyclization reaction. This method involves simple work up and amenable for large scale preparations. The heterogeneous acid treated catalyst can be regenerated and used for up to three cycles with minimum loss of activity.

Synthesis and antifungal activity of some thiazole derivatives

A series of some thiazole derivatives were designed and synthesized. The structure of newly synthesized compounds was characterized by HRMS, 1H NMR and 13C NMR. The synthesized compounds were evaluated against ten species of fungi in vitro by agar cup plate and micro-titration methods, respectively. The results of antifungal screening reveal that among all the compounds screened three compounds showed moderate antifungal activity. The MIC value of 3 h against two fungal strains C. neoformans and C. albicas is 8 μg mL-1 respectively. The MIC value of 3i against two fungal strains C. neoformans and T. mentagrophytes is 8 μg mL-1 and 16 μg mL-1, respectively and 3a against T. mentagrophytes is 16 μg mL-1, the MIC of others are all beyond 32 μg mL-1.

Novel thiazolidine derivatives

The invention relates to with novel thiazolidine derivatives of the formula STR1 wherein X is methylene, oxygen or sulfur; R1 is halogen; R2 is hydrogen, nitro, cyano, OR3 or NHR3 ; or R1 and R2 both simultaneously are hydrogen or nitro; R3 is hydrogen, alkyl, acyl, --CO--OR4 or --CO--NHR4 ; and R4 is alkyl, unsubstituted or substituted aryl or aralkyl, and their salts with physiologically compatible cations. The compounds of formula I are useful in the treatment of metabolic disorders.