Basic information Safety Supplier Related

2,3-DIFLUORO-4-METHOXYBENZOIC ACID

Basic information Safety Supplier Related

2,3-DIFLUORO-4-METHOXYBENZOIC ACID Basic information

Product Name:
2,3-DIFLUORO-4-METHOXYBENZOIC ACID
Synonyms:
  • 2,3-Difluoro-4-methoxylbenzoic acid
  • 2,3-Difluoro-6-methoxybenzoic acid
  • Benzoic acid, 2,3-difluoro-6-methoxy-
CAS:
773873-26-0
MF:
C8H6F2O3
MW:
188.13
Product Categories:
  • Aromatic Halides (substituted)
  • Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts
  • Benzoic acid
Mol File:
773873-26-0.mol
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2,3-DIFLUORO-4-METHOXYBENZOIC ACID Chemical Properties

Melting point:
126-129°C
Boiling point:
275.0±35.0 °C(Predicted)
Density 
1.399±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
2.82±0.10(Predicted)
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Safety Information

Hazard Codes 
Xi
Hazard Note 
Irritant
HS Code 
2918999090
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2,3-DIFLUORO-4-METHOXYBENZOIC ACID Usage And Synthesis

Synthesis

187543-87-9

773873-26-0

General procedure for the synthesis of 2,3-difluoro-6-methoxybenzoic acid from 2,3-difluoro-6-methoxybenzaldehyde: 1. Preparation of reaction system: 2,3-difluoro-6-methoxybenzaldehyde (0.5 g, 2.91 mmol) was suspended in potassium hydroxide solution (3 g KOH dissolved in 20 ml of water). 2. Oxidizing reaction: hydrogen peroxide solution (27.5% w/w, 4 ml) was added to the above suspension, followed by heating the reaction at 70°C for 2 hours. 3. Acidification: after completion of the reaction, the reaction mixture was acidified to pH 2 with concentrated hydrochloric acid. 4. Extractive separation: the acidified reaction mixture was washed with ethyl acetate. 5. Drying and concentration: the organic phases were combined, dried with anhydrous magnesium sulfate, filtered and the solvent was evaporated in vacuum. 6. Purification: Further purification by azeotropy with toluene afforded 2,3-difluoro-6-methoxybenzoic acid as a white solid (500 mg, 91% yield). Remarks: LC/MS analysis showed a retention time of 12.08 min and no molecular ion peak was observed.

References

[1] Patent: WO2006/77414, 2006, A1. Location in patent: Page/Page column 148
[2] Patent: CN105523921, 2016, A. Location in patent: Paragraph 0014; 0015; 0016

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