2-(4-fluorophenyl)propionic acid

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Products Intro: Product Name:2-(4-Fluorophenyl)propanoic Acid
CAS:75908-73-5
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CAS:75908-73-5
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Products Intro: Product Name:2-(4-fluorophenyl)propionic acid
CAS:75908-73-5
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2-(4-fluorophenyl)propionic acid manufacturers

2-(4-fluorophenyl)propionic acid Basic information
Product Name:2-(4-fluorophenyl)propionic acid
Synonyms:2-(4-fluorophenyl)propionic acid;4-Fluoro-alpha-methylphenylaceticacid;2-(4-Fluorophenyl)propanoic acid;4-Fluoro-α-methylbenzeneacetic acid;4-Fluoro-alpha-methylphenylacetic acid,98%;(+/-)-2-(4-flurophenyl)propanoic acid;Benzeneacetic acid, 4-fluoro-α-methyl-;Benzeneacetic acid,4-fluoro-a-methyl-
CAS:75908-73-5
MF:C9H9FO2
MW:168.16
EINECS:278-340-6
Product Categories:
Mol File:75908-73-5.mol
2-(4-fluorophenyl)propionic acid Structure
2-(4-fluorophenyl)propionic acid Chemical Properties
Boiling point 258.8±15.0 °C(Predicted)
density 1+-.0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
pka4.31±0.10(Predicted)
color Off-white
Safety Information
RIDADR 2811
HazardClass 6.1
PackingGroup 
HS Code 2918199890
MSDS Information
2-(4-fluorophenyl)propionic acid Usage And Synthesis
Synthesis
methyl 2-(4-fluorophenyl)propanoate

50415-71-9

2-(4-fluorophenyl)propionic acid

75908-73-5

The general procedure for the synthesis of 2-(4-fluorophenyl)propionic acid from the compound (CAS: 50415-71-9) was as follows: under stirring conditions, racemic methyl 2-(4-thieno-phenyl)propionate (18.9 g) was dissolved in ethanol (200 mL) and an aqueous solution of potassium hydroxide (35 g) (200 mL) was slowly added. The reaction mixture was stirred continuously at 0 °C for 4 hours. Upon completion of the reaction, the pH was adjusted to 5 with 4.0 M hydrochloric acid, followed by extraction of the reaction mixture with ethyl acetate. The organic phase was separated and the solvent was removed by distillation under reduced pressure to give 15.64 g of 2-(4-fluorophenyl)propionic acid as a crude product. The crude product could be used directly in the subsequent reaction without further purification. The structure of the product was confirmed by 1H-NMR (300 MHz, DMSO-d6): δ [ppm] = 1.31 (d, 3H), 3.66 (q, 1H), 7.05-7.15 (m, 2H), 7.24-7.33 (m, 2H), 12.30 (s, 1H).

References[1] Organic letters, 2002, vol. 4, # 3, p. 371 - 373
[2] Journal of Organic Chemistry, 2003, vol. 68, # 19, p. 7234 - 7242
[3] Patent: WO2010/31183, 2010, A1. Location in patent: Page/Page column 18
[4] Patent: WO2013/87579, 2013, A1. Location in patent: Page/Page column 134; 135
[5] Patent: WO2014/9219, 2014, A1. Location in patent: Page/Page column 107; 108
2-(4-fluorophenyl)propionic acid Preparation Products And Raw materials
Raw materialsmethyl 2-(4-fluorophenyl)propanoate-->Water-->Ethanol-->Potassium hydroxide
Tag:2-(4-fluorophenyl)propionic acid(75908-73-5) Related Product Information
(S)-2-(4-FLUOROPHENYL) 3-METHYLBUTYRIC ACID 1-(4-FLUOROPHENYL)CYCLOPENTANECARBOXYLIC ACID, 98 1-(2-CHLORO-4-FLUOROPHENYL)CYCLOPENTANECARBOXYLIC ACID, 98 2-(4-FLUOROPHENYL)SUCCINIC ACID 2-Pentafluorophenyl-malonic acid diethyl ester 2-(4-FLUOROPHENYL)ISOVALERIC ACID 2-AMINO-2-(4-FLUORO-PHENYL)-PROPIONIC ACID 2-AMINO-2-(4-FLUOROPHENYL)BUTANOIC ACID 2-(4-FLUOROPHENYL)-2-PHENYLACETIC ACID DIETHYL 2,4-DIFLUOROPHENYL MALONATE 2-(4-fluorophenyl)propionic acid 2-(4-FLUOROPHENYL)-4-(3-METHOXYPHENYL)-4-OXOBUTANOIC ACID 1-(2-CHLORO-4-FLUOROPHENYL)CYCLOHEXANECARBOXYLIC ACID 1-(4-FLUOROPHENYL)CYCLOHEXANECARBOXYLIC ACID, 98 RARECHEM AK ML 0153 RARECHEM AK ML 0161 METHYL 2-(4-FLUOROPHENYL)-4-(3-METHOXYPHENYL)-4-OXOBUTANOATE 4-(4-CHLOROPHENYL)-2-(4-FLUOROPHENYL)-4-OXOBUTANOIC ACID