459-31-4

Basic information

• Product Name: 3-(4-FLUOROPHENYL)PROPIONIC ACID
• Synonyms: AKOS BC-2700;3-(4-FLUOROPHENYL)PROPANOIC ACID;3-(4-FLUOROPHENYL)PROPIONIC ACID;3-(4-FLUOROPHENYL)PROPRIONIC ACID;3-(4-fluorobenzene)propionic acid;3-(4-Fluorophenyl)propionic acid 97%;3-(4-Fluorophenyl)propionicacid97%;3-(4-Fluorophenyl)propionic acid,98%
• CAS NO: 459-31-4
• Molecular Formula: C₉H₉FO₂
• Molecular Weight: 168.16
• EINECS: -0
• Product Categories: Aromatic Propionic Acids;C9;Carbonyl Compounds;Carboxylic Acids
• Mol File: 459-31-4.mol
• Article Data: 33

Chemical Properties

• Melting Point: 86-91 °C(lit.)
• Boiling Point: 278.9 °C at 760 mmHg
• Flash Point: 122.5 °C
• Appearance: White to off-white/Crystalline Powder or Crystals
• Density: 1.222 g/cm³
• Vapor Pressure: 0.00199mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• Solubility: slightly sol. in Methanol
• PKA: 4?+-.0.10(Predicted)
• BRN: 1869084
• CAS DataBase Reference: 3-(4-FLUOROPHENYL)PROPIONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-FLUOROPHENYL)PROPIONIC ACID(459-31-4)
• EPA Substance Registry System: 3-(4-FLUOROPHENYL)PROPIONIC ACID(459-31-4)

Safety Data

• Hazard Codes: C,Xi
• Statements: 34-36/37/38
• Safety Statements: 45-36/37/39-26-37/39
• WGK Germany: 3
• HazardClass: IRRITANT
• Hazardous Substances Data: 459-31-4(Hazardous Substances Data)

Usage

Chemical Properties

white to off-white crystalline powder or crystals

Uses

3-(4-Fluorophenyl)propionic acid may be used in the synthesis of 2-oxopiperazine guanidine analog.

InChI:InChI=1/C9H9FO2/c10-8-4-1-7(2-5-8)3-6-9(11)12/h1-2,4-5H,3,6H2,(H,11,12)/p-1

Upstream product

• 459-46-1 4-Fluorobenzyl bromide 
• 105-53-3 diethyl malonate 
• 405-99-2 para-fluorostyrene 
• 3495-36-1 cesium formate 
• 141-82-2 malonic acid 
• 459-57-4 4-fluorobenzaldehyde 
• 64-18-6 formic acid 
• 124-38-9 carbon dioxide 
• 332-42-3 (2-bromoethyl)-4-fluorobenzene 
• 136265-10-6 ethyl 4-fluorocinnamate 
• 201230-82-2 carbon monoxide 
• 352-34-1 4-fluoro-1-iodobenzene 
• 802294-64-0 propionic acid 
• 702-15-8 3-(4-fluorophenyl)propan-1-ol 

Downstream Products

• 174485-36-0 3-(4-fluorophenyl)-N-methoxy-N-methylpropanamide 
• 457948-39-9 C₁₆H₁₆FNO₂ 
• 777952-97-3 3-[5-(4-fluorophenyl)-3-oxo-pentanoyl]benzonitrile 
• 459872-39-0 N-[3-(4-fluorophenyl)propyl]-N-methylamine 
• 852661-70-2 N-cyclopropyl-3-(4-fluorophenyl)propylamine 
• 852660-77-6 3-(4-fluorophenyl)-N-propylpropan-1-amine 
• 852661-58-6 [3-(4-fluorophenyl)propyl](2,2,2-trifluoroethyl)amine 
• 852661-63-3 (2S,3R)-3-amino-1-[[3-(4-fluorophenyl)propyl](methyl)amino]butan-2-ol 
• 852661-60-0 (2S,3R)-3-amino-1-[[3-(4-fluorophenyl)propyl](2,2,2-trifluoroethyl)amino]butan-2-ol 
• 852661-68-8 (2S,3R)-3-amino-1-{cyclohexyl[3-(4-fluorophenyl)propyl]amino}butan-2-ol 
• 852661-62-2 (2S,3R)-3-(dibenzylamino)-1-[[3-(4-fluorophenyl)propyl](methyl)amino]butan-2-ol 
• 852661-61-1 N-{(1R,2S)-3-[3-(4-fluorophenyl)propyl](methyl)amino-2-hydroxy-1-methylpropyl}-N'-[3-(1-methyl-1H-tetrazol-5-yl)phenyl]urea 
• 852661-59-7 (2S,3R)-3-(dibenzylamino)-1-[[3-(4-fluorophenyl)propyl](2,2,2-trifluoroethyl)amino]butan-2-ol 
• 852660-32-3 N-((1R,2S)-2-{[[3-(4-fluorophenyl)propyl]amino]methyl}cyclohexyl)-N'-[3-(1-methyl-1H-tetrazol-5-yl)phenyl]urea 

Relevant articles and documents

Photoredox Activation of Formate Salts: Hydrocarboxylation of Alkenes via Carboxyl Group Transfer

A photoredox activation mode of formate salts for carboxylation was developed. Using a formate salt as the reductant, carbonyl source, and hydrogen atom transfer reagent, a wide range of alkenes can be converted into acid products via a carboxyl group tra

Method for synthesizing phenylpropionic acid compounds through heterogeneous palladium metal catalysis

The invention discloses a method for synthesizing phenylpropionic acid compounds by heterogeneous catalysis. The method comprises the following steps: sequentially adding Pd@POL, toluene, styrene, formic acid and acetic anhydride into a reaction flask, stirring the reaction mixture at 80 DEG C to react, cooling the reaction solution to room temperature after the reaction is finished, diluting with dichloromethane, and transferring the solution into a separating funnel, washing with a sodium hydroxide solution, acidifying the water layer with a hydrochloric acid aqueous solution, extracting with dichloromethane, merging organic phases, drying with anhydrous sodium sulfate, and carrying out vacuum concentration to obtain the phenylpropionic acid compound. The method can remove heavy metal residues, is green and environment-friendly, is simple to operate and easy to implement, and the prepared phenylpropionic acid compound has a good application prospect.

Hydrogenation reaction method

The invention relates to a hydrogenation reaction method, and belongs to the technical field of organic synthesis. The hydrogenation reaction method provided by the invention comprises the following steps: carrying out a hydrogen transfer reaction on a hydrogen acceptor compound, pinacol borane and a catalyst in a solvent in the presence of proton hydrogen, so that the hydrogen acceptor compound is subjected to a hydrogenation reaction; the catalyst is one or more than two of a palladium catalyst, an iridium catalyst and a rhodium catalyst; the hydrogen acceptor compound comprises one or morethan two functional groups of carbon-carbon double bonds, carbon-carbon triple bonds, carbon-oxygen double bonds, carbon-nitrogen double bonds, nitrogen-nitrogen double bonds, nitryl, carbon-nitrogentriple bonds and epoxy. The method is mild in reaction condition, easy to operate, high in yield, short in reaction time, wide in substrate application range, suitable for carbon-carbon double bonds,carbon-carbon triple bonds, carbon-oxygen double bonds, carbon-nitrogen double bonds, nitrogen-nitrogen double bonds, nitryl, carbon-nitrogen triple bonds and epoxy functional groups, good in selectivity and high in reaction specificity.