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4-FLUORO-3-METHOXYBENZOIC ACID

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CAS:82846-18-2
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CAS:82846-18-2
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CAS:82846-18-2
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Products Intro: Product Name:4-Fluoro-3-methoxybenzoic acid
CAS:82846-18-2
Purity:98% Package:1KG;10KG;50KG

4-FLUORO-3-METHOXYBENZOIC ACID manufacturers

4-FLUORO-3-METHOXYBENZOIC ACID Basic information
Product Name:4-FLUORO-3-METHOXYBENZOIC ACID
Synonyms:RARECHEM AL BO 0973;4-FLUORO-3-METHOXYBENZOIC ACID;Fluoro-3-methoxy-benzoic acid;4-Fluoro-m-anisic acid, 5-Carboxy-2-fluoroanisole;3-METHOXY-4-FLUOROBENZOIC ACID;4-fluoro-m-anisic acid;BUTTPARK 14\01-28;4-Fluoro-3-methoxybenzoic
CAS:82846-18-2
MF:C8H7FO3
MW:170.14
EINECS:
Product Categories:Fluorine series;Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;Carboxylic Acids;Phenyls & Phenyl-Het;Acids & Esters;Anisoles, Alkyloxy Compounds & Phenylacetates;Fluorine Compounds;Carboxylic Acids;Phenyls & Phenyl-Het
Mol File:82846-18-2.mol
4-FLUORO-3-METHOXYBENZOIC ACID Structure
4-FLUORO-3-METHOXYBENZOIC ACID Chemical Properties
Melting point 206 °C
Boiling point 304.8±22.0 °C(Predicted)
density 1.307±0.06 g/cm3(Predicted)
Fp >110℃
storage temp. Sealed in dry,Room Temperature
pka4.02±0.10(Predicted)
form powder to crystal
color White to Yellow to Orange
BRN 4178071
InChIKeyLWGCZCMLPRMKIZ-UHFFFAOYSA-N
CAS DataBase Reference82846-18-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-36:37/38-22
Safety Statements 26-36-37
Hazard Note Irritant
HS Code 29189900
MSDS Information
ProviderLanguage
ALFA English
4-FLUORO-3-METHOXYBENZOIC ACID Usage And Synthesis
Chemical PropertiesWhite to light yellow crystal powder
Synthesis Reference(s)Journal of Medicinal Chemistry, 33, p. 2408, 1990 DOI: 10.1021/jm00171a014
Synthesis
Methyl 4-fluoro-3-Methoxybenzoate

74385-37-8

4-FLUORO-3-METHOXYBENZOIC ACID

82846-18-2

The general procedure for the synthesis of 3-methoxy-4-fluorobenzoic acid from methyl 4-fluoro-3-methoxybenzoate was as follows: methyl 4-fluoro-3-methoxybenzoate (11 g, 59.8 mmol) was dissolved in methanol (100 mL), and a solution of sodium hydroxide (9.5 g, 240 mmol) in water (20 mL) was added, and the reaction was stirred for 4 h at room temperature. Upon completion of the reaction, the solvent was removed by distillation under reduced pressure to give a residue. The residue was dissolved in water (100 mL) and the pH was adjusted with 1N HCl solution to 4. Subsequently, the precipitated solid was collected by filtration, washed with water (3 x 50 mL), and dried to give 3-methoxy-4-fluorobenzoic acid as a white solid (9 g, 97% yield). The product was characterized by 1H-NMR (300 MHz, DMSO-d6): δ 7.66-7.55 (m, 2H), 7.37-7.30 (m, 1H), 3.91 (s, 3H).

References[1] Patent: WO2014/66795, 2014, A1. Location in patent: Paragraph 0175
[2] Patent: US2004/204427, 2004, A1. Location in patent: Page/Page column 42
Tag:4-FLUORO-3-METHOXYBENZOIC ACID(82846-18-2) Related Product Information
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