5-METHOXYPYRIDINE-2-CARBOXYLIC ACID
5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Basic information
- Product Name:
- 5-METHOXYPYRIDINE-2-CARBOXYLIC ACID
- Synonyms:
-
- 5-METHOXYPICOLINIC ACID
- 5-METHOXYPYRIDINE-2-CARBOXYLIC ACID
- 5-METHOXY-2-PYRIDINECARBOXYLIC ACID
- 5-METHOXYPYRIDINE-2-CARBOXYLIC ACID, 98+%
- 5-METHOXYPYRIDINE-2-CARBOXLIC ACID
- 5-Methoxypyridine-2-carboxylic acid 5-Methoxy-2-pyridinecarboxylic acid
- 5-Methoxy-2-pyridinecarboxylic acid, 95+%
- 5-Methoxy-2-pyridinecarboxyL
- CAS:
- 29082-92-6
- MF:
- C7H7NO3
- MW:
- 153.14
- EINECS:
- 1533716-785-6
- Product Categories:
-
- Pyridines
- Heterocycle-Pyridine series
- Amino Acids & Derivatives
- Aromatics
- Mol File:
- 29082-92-6.mol
5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Chemical Properties
- Melting point:
- 172-174 °C
- Boiling point:
- 312.9±22.0 °C(Predicted)
- Density
- 1.284±0.06 g/cm3(Predicted)
- storage temp.
- Inert atmosphere,Room Temperature
- pka
- 1.07±0.50(Predicted)
5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Usage And Synthesis
Uses
A natural imino acid.
Synthesis
29681-39-8
29082-92-6
B) Synthesis of 5-methoxypyridine-2-carboxylic acid: a solution of lithium hydroxide monohydrate (5.0 g) in water (10 mL) was added to a solution of methyl 5-methoxypyridine-2-carboxylate (4.0 g) in methanol (50 mL) at room temperature. The reaction mixture was stirred at room temperature for 12 hours. Subsequently, the pH of the reaction mixture was adjusted to 4-5 with 2M hydrochloric acid and the precipitate was collected by filtration. The resulting solid was washed with water and dried to afford the target compound 5-methoxypyridine-2-carboxylic acid (2.4 g). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6): δ 3.93 (3H, s), 7.49-7.51 (1H, m), 8.03 (1H, d, J = 7.2 Hz), 8.36 (1H, d, J = 2.8 Hz), 12.85 (1H, s).
References
[1] Patent: EP2848618, 2015, A1. Location in patent: Paragraph 0707
5-METHOXYPYRIDINE-2-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials
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5-METHOXYPYRIDINE-2-CARBOXYLIC ACID(29082-92-6)Related Product Information
- 5-METHOXY-PYRIDIN-3-OL
- (5-METHOXYPYRIDIN-2-YL)METHANOL
- 5-METHOXYPICOLINALDEHYDE
- 5-Methoxypyridine-3-boronic acid
- 5-METHOXY-PYRIDINE-3-CARBALDEHYDE
- 5-METHOXYPYRIDINE-2-CARBOXYLIC ACID
- 2-CHLORO-6-METHOXYPYRIDINE-4-CARBOXYLIC ACID
- 6-Bromo-5-methoxypicolinic acid
- 2-methoxypyridine-3-carboxylic acid
- 3-Amino-6-methoxypyridine-2-carboxylic acid
- 5-Methoxy-3-pyridinemethanamine
- 5-(tert-Butoxycarbonylamino)-2-methoxypyridine-4-carboxylic acid ,97%,5-(TERT-BUTOXYCARBONYLAMINO)-2-METHOXYPYRIDINE-4-CARBOXYLIC ACID
- 5-Bromo-2-methoxypyridine-3-carboxylic acid
- 5-AMINO-2-METHOXYPYRIDINE-4-CARBOXYLIC ACID
- 4-CHLORO-3-METHOXYPYRIDINE-2-CARBOXYLIC ACID
- 4-Methoxypyridine-2-carboxylic acid 98%,4-METHOXYPYRIDINE-2-CARBOXYLIC ACID,4-Methoxypyridine-2-carboxylic acid ,97%
- 2-METHOXYPYRIDINE-5-CARBOXYLIC ACID
- 2-METHOXYPYRIDINE-4-CARBOXYLIC ACID