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2-Methoxy-4-pyridinecarboxylic acid

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2-Methoxy-4-pyridinecarboxylic acid Basic information
Product Name:2-Methoxy-4-pyridinecarboxylic acid
Synonyms:2-METHOXYISONICOTINIC ACID;2-METHOXYPYRIDINE-4-CARBOXYLIC ACID;2-METHOXY-4-PYRIDINECARBOXYLIC ACID;4-Pyridinecarboxylicacid,2-methoxy-(9CI);2-METHOXYISONICOTONIC ACID;4-METHOXY-4-PYRIDINECARBOXYLIC ACID;2-Methoxy-4-pyridinecarboxylic acid 2-Methoxyisonicotinic acid;2-Methoxypyridine-4-carboxylic acid 97%
CAS:105596-63-2
MF:C7H7NO3
MW:153.14
EINECS:
Product Categories:Pyridine;CARBOXYLICACID;blocks;Carboxes;Pyridines
Mol File:105596-63-2.mol
2-Methoxy-4-pyridinecarboxylic acid Structure
2-Methoxy-4-pyridinecarboxylic acid Chemical Properties
Melting point 198-200 °C
Boiling point 383.0±22.0 °C(Predicted)
density 1.284±0.06 g/cm3(Predicted)
storage temp. Keep in dark place,Sealed in dry,Room Temperature
form Solid or Crystalline Powder
pka4.50±0.10(Predicted)
color White to pale brown
InChIInChI=1S/C7H7NO3/c1-11-6-4-5(7(9)10)2-3-8-6/h2-4H,1H3,(H,9,10)
InChIKeyDPNDWFVORIGXQO-UHFFFAOYSA-N
SMILESC1(OC)=NC=CC(C(O)=O)=C1
CAS DataBase Reference105596-63-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38-36
Safety Statements 26-36/37/39
WGK Germany 3
HazardClass IRRITANT
HS Code 29333990
Storage Class11 - Combustible Solids
Hazard ClassificationsEye Irrit. 2
MSDS Information
2-Methoxy-4-pyridinecarboxylic acid Usage And Synthesis
Uses2-Methoxy-4-pyridinecarboxylic acid is often used as an intermediate in pharmaceutical chemistry and organic synthesis. In organic synthesis transformation, the carboxyl group on the pyridine ring can be converted into acyl chloride, ester group and amide under certain reaction conditions without being affected by the pyridine ring, and can also be reduced to a hydroxyl group.
Synthesis
2-Chloro-6-methoxyisonicotinic acid

15855-06-8

2-Methoxy-4-pyridinecarboxylic acid

105596-63-2

General procedure for the synthesis of 2-methoxy-4-pyridinecarboxylic acid from 2-chloro-6-methoxyisonicotinic acid: To a suspension of acetonitrile (150 mL) containing 2-methoxy-4-pyridinecarboxylic acid (1.94 g, 6.49 mmol) was added sodium iodide (4.90 g, 32.69 mmol) and trimethylmethylsilyl chloride (4.10 mL, 32.42 mmol). The reaction mixture was stirred at 40 °C for 3 days under nitrogen protection. After completion of the reaction, the mixture was cooled to 0 °C, the solid product was collected by filtration, washed with acetonitrile and dried to afford 1.66 g (90% yield) of the target compound, 2-methoxy-4-pyridinecarboxylic acid.LRMS: m/z 285 (M + 1)+; retention time: 2.86 min (Method B).

References[1] Patent: WO2010/43377, 2010, A1. Location in patent: Page/Page column 64
[2] Yakugaku Zasshi, 1953, vol. 73, p. 845,846, 847
[3] Chem.Abstr., 1954, p. 10021
Tag:2-Methoxy-4-pyridinecarboxylic acid(105596-63-2) Related Product Information
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