ChemicalBook--->CAS DataBase List--->3998-88-7

3998-88-7

3998-88-7 Structure

3998-88-7 Structure
IdentificationBack Directory
[Name]

Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
[CAS]

3998-88-7
[Synonyms]

2-Chloro-6-methylisonicotinic Acid Ethyl Ester
Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
2-Chloro-6-methylpyridine-4-carboxylic acid ethyl ester
4-Pyridinecarboxylic acid, 2-chloro-6-Methyl-, ethyl ester
JR-14076, Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%
[Molecular Formula]

C9H10ClNO2
[MDL Number]

MFCD09842151
[MOL File]

3998-88-7.mol
[Molecular Weight]

199.63
Chemical PropertiesBack Directory
[Melting point ]

65-67°C
[Boiling point ]

107°C/1.5mm
[density ]

1?+-.0.06 g/cm3(Predicted)
[Fp ]

107°C/1.5mm
[storage temp. ]

Inert atmosphere,Room Temperature
[solubility ]

soluble in Methanol
[form ]

powder to crystal
[pka]

-0.14±0.10(Predicted)
[color ]

White to Almost white
[InChI]

1S/C9H10ClNO2/c1-3-13-9(12)7-4-6(2)11-8(10)5-7/h4-5H,3H2,1-2H3
[InChIKey]

UMAAIDIASQFLTF-UHFFFAOYSA-N
[SMILES]

O=C(OCC)C1=CC(Cl)=NC(C)=C1
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[WGK Germany ]

WGK 3
[HS Code ]

2933399990
[Storage Class]

11 - Combustible Solids
Spectrum DetailBack Directory
[Spectrum Detail]

Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%(3998-88-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Chloro-6-methylpyridine-4-carboxylic acid

25462-85-5

Ethanol

64-17-5

Ethyl 2-chloro-6-methylpyridine-4-carboxylate, 97%

3998-88-7

Step 1: Synthesis of ethyl 2-chloro-6-methylisonicotinate (97). Concentrated sulfuric acid (2 mL) was added dropwise to a stirred solution of 2-chloro-6-methylpyridine-4-carboxylic acid (7.0 g, 40.79 mmol) in ethanol (70 mL) at 0 °C. Subsequently, the reaction mixture was heated to 80 °C and kept for 12 hours. Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under vacuum to remove the solvent. The concentrated residue was diluted with ethyl acetate and washed sequentially with water, sodium bicarbonate solution and saturated aqueous sodium chloride solution. The organic layer was separated, dried over anhydrous sodium sulfate, filtered and concentrated to give ethyl 2-chloro-6-methylisonicotinate (97) (7 g, 86% yield) as a white solid.

[References]

[1] Patent: US2010/249071, 2010, A1. Location in patent: Page/Page column 63-64
[2] Patent: WO2008/29371, 2008, A1. Location in patent: Page/Page column 41
[3] Patent: WO2009/24905, 2009, A1. Location in patent: Page/Page column 38-39; 49
[4] Patent: US2010/63108, 2010, A1. Location in patent: Page/Page column 16
[5] Patent: US2011/46170, 2011, A1. Location in patent: Page/Page column 17
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