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75358-89-3

75358-89-3 Structure

75358-89-3 Structure
IdentificationBack Directory
[Name]

2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
[CAS]

75358-89-3
[Synonyms]

Methyl 2-Cyanopyridine-3-carboxylate
2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER
3-Pyridinecarboxylic acid, 2-cyano-, methyl ester
2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER ISO 9001:2015 REACH
[Molecular Formula]

C8H6N2O2
[MDL Number]

MFCD00128863
[MOL File]

75358-89-3.mol
[Molecular Weight]

162.15
Chemical PropertiesBack Directory
[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
Safety DataBack Directory
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER(75358-89-3)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-(AMINOCARBONYL)NICOTINIC ACID

5860-70-8

Methyl chloroformate

79-22-1

2-CYANO-3-PYRIDINECARBOXYLIC ACID METHYL ESTER

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
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