5-BROMO-1-METHYL-2(1H)-PYRIDINONE

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Products Intro: Product Name:5-Bromo-1-methylpyridin-2(1H)-one
CAS:81971-39-3
Purity:>95% Package:1g;5g;10g;25g;100g
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Products Intro: Product Name:5-Bromo-1-methylpyridin-2(1H)-one
CAS:81971-39-3
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-56697
Company Name: Wuhan Chemwish Technology Co., Ltd
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Products Intro: Product Name:5-Bromo-1-methylpyridin-2(1H)-one
CAS:81971-39-3
Purity:0.98 Package:1g;5g;25g;3377g
Company Name: Shenzhen Excellent Biotech Co., Ltd.
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Products Intro: Product Name:5-bromo-1-methylpyridone
CAS:81971-39-3
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Products Intro: Product Name:5-BROMO-1-METHYL-2(1H)-PYRIDINONE
CAS:81971-39-3
Purity:99% Package:1KG;1USD

5-BROMO-1-METHYL-2(1H)-PYRIDINONE manufacturers

5-BROMO-1-METHYL-2(1H)-PYRIDINONE Basic information
Product Name:5-BROMO-1-METHYL-2(1H)-PYRIDINONE
Synonyms:5-bromo-1-methyl-1,2-dihydropyridin-2-one;5-Bromo-1-methylpyridin-2(1H)-one;5-BROMO-1-METHYL-2(1H)-PYRIDINONE;5-BroMo-1-Methyl-1H-pyridin-2-one;5-BroMo-1-Methylpyridin-2...;3-Bromo-1-methyl-6-oxo-1,6-dihydropyridine;5-Bromo-1-methyl-2(1H)-pyridone;5-Bromo-1-methyl-pyridin-2-one
CAS:81971-39-3
MF:C6H6BrNO
MW:188.02
EINECS:
Product Categories:
Mol File:81971-39-3.mol
5-BROMO-1-METHYL-2(1H)-PYRIDINONE Structure
5-BROMO-1-METHYL-2(1H)-PYRIDINONE Chemical Properties
Melting point 62-63℃
Boiling point 258℃
density 1.664
Fp 110℃
storage temp. Inert atmosphere,Room Temperature
pka-0.41±0.62(Predicted)
form powder to crystal
color White to Yellow to Orange
InChIInChI=1S/C6H6BrNO/c1-8-4-5(7)2-3-6(8)9/h2-4H,1H3
InChIKeyHHVFVHIUOMMWRN-UHFFFAOYSA-N
SMILESC1(=O)N(C)C=C(Br)C=C1
Safety Information
HS Code 2933399990
MSDS Information
5-BROMO-1-METHYL-2(1H)-PYRIDINONE Usage And Synthesis
Synthesis
2-Hydroxy-5-bromopyridine

13466-38-1

Iodomethane

74-88-4

5-BROMO-1-METHYL-2(1H)-PYRIDINONE

81971-39-3

5-Bromopyridin-2(1H)-one (8.6 g, 0.05 mol) was dissolved in THF (120 mL) at 0 °C and slowly added to a suspension of NaH (4.8 g, 0.2 mol) in THF (10 mL). The reaction mixture was stirred at 0 °C for 1 hour. Subsequently, iodomethane (35.5 g, 0.25 mol) was added dropwise to the mixture and stirring was continued for 3 hours at room temperature. After completion of the reaction, the reaction was quenched with saturated aqueous NH4Cl solution. The organic phase was separated and concentrated to give the crude product. The crude product was purified by column chromatography to afford 5-bromo-1-methylpyridin-2(1H)-one (8.9 g, 96.78% yield).1H NMR (CDCl3): δ= 3.5 (s, 3H), 6.52 (m, 1H), 7.32 (m, 1H), 7.45 (m, 1H).

References[1] Patent: US2010/331320, 2010, A1. Location in patent: Page/Page column 56
[2] Bioorganic and Medicinal Chemistry, 2017, vol. 25, # 14, p. 3649 - 3657
[3] Synlett, 2015, vol. 26, # 11, p. 1557 - 1562
[4] Patent: WO2013/49559, 2013, A1. Location in patent: Page/Page column 68
[5] Patent: WO2005/44195, 2005, A2. Location in patent: Page/Page column 40
Tag:5-BROMO-1-METHYL-2(1H)-PYRIDINONE(81971-39-3) Related Product Information
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