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ChemicalBook--->CAS DataBase List--->62774-90-7

62774-90-7

62774-90-7 Structure

62774-90-7 Structure
IdentificationBack Directory
[Name]

2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid
[CAS]

62774-90-7
[Synonyms]

62774-90-7
2,6-dichloro-4-methylnicotinic acid
2,6-Dichloro-4-methylnicotinicacid,98%
2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid
2,6-dichloro-4-methylpyridine-3-carboxylic acid
3-Pyridinecarboxylic acid, 2,6-dichloro-4-Methyl-
[Molecular Formula]

C7H5Cl2NO2
[MDL Number]

MFCD02932724
[MOL File]

62774-90-7.mol
[Molecular Weight]

206.03
Chemical PropertiesBack Directory
[Melting point ]

140-141 °C
[Boiling point ]

370.1±37.0 °C(Predicted)
[density ]

1.522±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

1.55±0.38(Predicted)
[Appearance]

White to light yellow Solid
[InChI]

InChI=1S/C7H5Cl2NO2/c1-3-2-4(8)10-6(9)5(3)7(11)12/h2H,1H3,(H,11,12)
[InChIKey]

QOSNTWMXACGOMD-UHFFFAOYSA-N
[SMILES]

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


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933399990
Spectrum DetailBack Directory
[Spectrum Detail]

2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid(62774-90-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

2,6-Dichloro-4-methylnicotinonitrile

875-35-4

2,6-Dichloro-4-methyl-3-pyridinecarboxylic acid

62774-90-7

Method 2: Concentrated nitric acid (14 mL) was slowly added to concentrated sulfuric acid (43 mL) that had been pre-cooled to 0°C, ensuring that the temperature of the reaction system was maintained below 10°C. The reaction system was then heated to 70°C. The reaction system was then heated to 70°C. After addition, the mixed acid solution was warmed to 70 °C, followed by the addition of commercially available 2,6-dichloro-4-methylnicotinonitrile (20.0 g, 107 mmol). The heating was continued until the internal temperature of the reaction system reached 105°C. The heating was stopped. After 2 hours of reaction, TLC monitoring showed complete reaction. The reaction mixture was cooled to room temperature and quenched by slowly pouring into ice (100 g) under vigorous stirring. The precipitated solid was collected by filtration and washed with cold water (10 mL). The resulting solid was dissolved in ethyl acetate (100 mL) and the solution was dried over anhydrous sodium sulfate and concentrated to give 2,6-dichloro-4-methylnicotinic acid (21.0 g, 96% yield) as a white solid: Rf = 0.20 (unfolding reagent ratio 1:1 ethyl acetate/hexane solvent mixture).

[References]

[1] Patent: US6677352, 2004, B1. Location in patent: Page/Page column 46
[2] Chemistry of Heterocyclic Compounds, 2004, vol. 40, # 3, p. 308 - 314
[3] Journal of Organic Chemistry, 2000, vol. 65, # 10, p. 3111 - 3115
[4] Patent: WO2016/33009, 2016, A1. Location in patent: Page/Page column 17
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