ChemicalBook--->CAS DataBase List--->189281-66-1

189281-66-1

189281-66-1 Structure

189281-66-1 Structure
IdentificationBack Directory
[Name]

METHYL 2,6-DICHLORO-5-FLUORONICOTINATE
[CAS]

189281-66-1
[Synonyms]

METHYL 2,6-DICHLORO-5-FLUORONICOTINATE
Methyl2,6-dichloro-5-fluoronicotinate97%
Methyl 2,6-dichloro-5-fluoropyridine-3-carboxylate
2,6-dichloro-5-fluoro-3-pyridinecarboxylic acid methyl ester
3-Pyridinecarboxylicacid, 2,6-dichloro-5-fluoro-, methyl ester
Methyl 2,6-dichloro-5-fluoropyridine-3-carboxylate, 2,6-Dichloro-3-fluoro-5-(methoxycarbonyl)pyridine
[Molecular Formula]

C7H4Cl2FNO2
[MDL Number]

MFCD02180634
[MOL File]

189281-66-1.mol
[Molecular Weight]

224.02
Chemical PropertiesBack Directory
[Boiling point ]

84 °C
[density ]

1.506±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-5.43±0.10(Predicted)
[Appearance]

Colorless to light yellow Liquid
[InChI]

InChI=1S/C7H4Cl2FNO2/c1-13-7(12)3-2-4(10)6(9)11-5(3)8/h2H,1H3
[InChIKey]

WADLLLSMEPLCNO-UHFFFAOYSA-N
[SMILES]

C1(Cl)=NC(Cl)=C(F)C=C1C(OC)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Environment (GHS09)
GHS07,GHS09
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H410
[Precautionary statements ]

P501-P273-P264-P280-P302+P352-P391-P337+P313-P305+P351+P338-P362+P364-P332+P313
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[Hazard Note ]

Irritant
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

METHYL 2,6-DICHLORO-5-FLUORONICOTINATE(189281-66-1)1HNMR
METHYL 2,6-DICHLORO-5-FLUORONICOTINATE(189281-66-1)FT-IR
Hazard InformationBack Directory
[Synthesis]

Methanol

67-56-1

2,6-Dichloro-5-fluoronicotinic acid

82671-06-5

METHYL 2,6-DICHLORO-5-FLUORONICOTINATE

189281-66-1

At 0°C, 2,6-dichloro-5-fluoropyridine-3-carboxylic acid (5 g, 23.8 mmol) was dissolved in methanol (50 ml) and thionyl chloride (5.66 g, 47.62 mmol) and 2 drops of DMF were added slowly [vigorous bulging was observed]. The reaction mixture was stirred at room temperature for 3 hours. Subsequently, methanol was added to the reaction system and stirring was continued for 2 hours at room temperature. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the residue was poured into ice-cold water (20 mL) and extracted with dichloromethane (2 x 50 mL). The organic layers were combined, washed sequentially with water and brine, and the solvent was evaporated under reduced pressure to afford methyl 2,6-dichloro-5-fluoropyridine-3-carboxylate (5 g, 93.8% yield).

[References]

[1] Patent: US2015/25087, 2015, A1. Location in patent: Paragraph 0168; 0198; 0199
[2] Patent: WO2016/51193, 2016, A1. Location in patent: Paragraph 00667; 00668; 00669
[3] Patent: TW2017/14884, 2017, A. Location in patent: Paragraph 0076
[4] Patent: EP2589592, 2018, B1. Location in patent: Paragraph 0563; 0564
[5] Patent: WO2010/126851, 2010, A1. Location in patent: Page/Page column 108-109
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