ChemicalBook > Product Catalog > Pharmaceutical intermediates > Heterocyclic compound > Pyridine compound > Cyanopyridine > 2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER Basic information
- Product Name:
- 2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
- Synonyms:
-
- 2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
- Methyl 2-Cyanopyridine-3-carboxylate
- 3-Pyridinecarboxylic acid, 2-cyano-, methyl ester
- 2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER ISO 9001:2015 REACH
- 2-Cyanopyridine-3-carboxylic acid methyl ester
- CAS:
- 75358-89-3
- MF:
- C8H6N2O2
- MW:
- 162.15
- Mol File:
- 75358-89-3.mol
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2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER Chemical Properties
- storage temp.
- Sealed in dry,Room Temperature
- Appearance
- White to off-white Solid
- InChI
- InChI=1S/C8H6N2O2/c1-12-8(11)6-3-2-4-10-7(6)5-9/h2-4H,1H3
- InChIKey
- ANPYBZGPGODWJD-UHFFFAOYSA-N
- SMILES
- C1(C#N)=NC=CC=C1C(OC)=O
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2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER Usage And Synthesis
Synthesis
5860-70-8
79-22-1
75358-89-3
2-Carbamoyl nicotinic acid (7.47 g, 45 mmol) was suspended in CH2Cl2 (50 mL) at 0°C and Et3N (13.08 mL, 94 mmol) and methyl chloroformate (7.65 mL, 99 mmol) were added sequentially under stirring. The reaction mixture was stirred at room temperature for 8 h. The reaction mixture was then diluted with CHCl3 (50 mL), washed sequentially with water, dried over MgSO4 and subsequently concentrated in vacuum. The product was washed with hexane and dried to give methyl 2-cyanopyridine-3-carboxylate.
References
[1] Synthesis (Germany), 2015, vol. 47, # 15, p. 2285 - 2293
2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTERSupplier
Zhimei (Shandong) Pharmaceutical Technology Co., Ltd Gold
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Suzhou bayaoke Biotechnology Co., Ltd Gold
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Wuhan Kaymke Chemical Co., Ltd.,
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2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER(75358-89-3)Related Product Information
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- METHYL 2-CYANO-6-METHOXYNICOTINATE
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- 2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER