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5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester

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Products Intro: Product Name:Methyl 5-Bromo-3-methylpicolinate
CAS:213771-32-5
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester
CAS:213771-32-5
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Products Intro: Product Name:Methyl 5-Bromo-3-methylpyridine-2-carboxylate
CAS:213771-32-5
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Products Intro: Product Name:5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester
CAS:213771-32-5
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Products Intro: Product Name:Methyl 5-bromo-3-methylpicolinate
CAS:213771-32-5
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-02823

5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester manufacturers

5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester Basic information
Product Name:5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester
Synonyms:5-BroMo-3-Methylpyridine-2-Carboxylic Acid Methyl;5-Bromo-3-methylpicolinic acid methyl ester;methyl 3-methyl-5-bromo-2-pyridinecarboxylate;Methyl 5-bromo-3-methylpicolinate, 5-Bromo-2-(methoxycarbonyl)-3-methylpyridine;2-Pyridinecarboxylic acid, 5-bromo-3-methyl-, methyl ester;Methyl 5-Bromo-3-methylpicolinate;Methyl 5-bromo-3-methyl-pyridine-2-carboxylate;5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester ISO 9001:2015 REACH
CAS:213771-32-5
MF:C8H8BrNO2
MW:230.06
EINECS:
Product Categories:Heterocycle-Pyridine series
Mol File:213771-32-5.mol
5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester Structure
5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester Chemical Properties
Boiling point 302.2±37.0 °C(Predicted)
density 1.503
storage temp. Inert atmosphere,Room Temperature
pka-0.17±0.10(Predicted)
AppearanceWhite to yellow Solid
InChIInChI=1S/C8H8BrNO2/c1-5-3-6(9)4-10-7(5)8(11)12-2/h3-4H,1-2H3
InChIKeyKZPOANNAYCXMSH-UHFFFAOYSA-N
SMILESC1(C(OC)=O)=NC=C(Br)C=C1C
Safety Information
HS Code 2933399990
MSDS Information
5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester Usage And Synthesis
Synthesis
5-BROMO-2-CARBOXY-3-METHYLPYRIDINE

886365-43-1

Iodomethane

74-88-4

5-Bromo-3-methylpyridine-2-carboxylic acid methyl ester

213771-32-5

Step C: Synthesis of methyl 5-bromo-3-methylpyridine-2-carboxylate 5-Bromo-3-methylpyridine-2-carboxylic acid (2.6 g, 12 mmol) was dissolved in N,N-dimethylformamide (20.0 mL) followed by addition of potassium carbonate (4.99 g, 36.1 mmol) and iodomethane (1.50 mL, 24.1 mmol). The reaction mixture was stirred at 80 °C for 40 min. After completion of the reaction, the mixture was extracted with ethyl acetate and water by partitioning. The organic layer was separated, washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated to give methyl 5-bromo-3-methylpyridine-2-carboxylate 2.3 g in yellow solid form in 83% yield.

References[1] Patent: US2013/96144, 2013, A1. Location in patent: Paragraph 0392; 0393
[2] Patent: WO2008/100715, 2008, A1. Location in patent: Page/Page column 34
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