2-BROMO-5-ETHOXYPYRIDINE
- Product Name
- 2-BROMO-5-ETHOXYPYRIDINE
- CAS No.
- 42834-01-5
- Chemical Name
- 2-BROMO-5-ETHOXYPYRIDINE
- Synonyms
- 2-BROMO-5-ETHOXYPYRIDINE;Pyridine, 2-bromo-5-ethoxy-
- CBNumber
- CB1501357
- Molecular Formula
- C7H8BrNO
- Formula Weight
- 202.05
- MOL File
- 42834-01-5.mol
2-BROMO-5-ETHOXYPYRIDINE Property
- Melting point:
- 49-49.5 °C
- Boiling point:
- 107 °C(Press: 33 Torr)
- Density
- 1.449±0.06 g/cm3(Predicted)
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- crystalline solid
- pka
- -2.22±0.10(Predicted)
- color
- White
Safety
- HS Code
- 2933399990
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- B696068
- Product name
- 2-Bromo-5-ethoxypyridine
- Packaging
- 1g
- Price
- $165
- Updated
- 2021/12/16
- Product number
- V5913
- Product name
- 2-Bromo-5-ethoxypyridine
- Packaging
- 5g
- Price
- $263
- Updated
- 2021/12/16
- Product number
- OR3575
- Product name
- 2-Bromo-5-ethoxypyridine
- Packaging
- 5g
- Price
- $319
- Updated
- 2021/12/16
- Product number
- OR3575
- Product name
- 2-Bromo-5-ethoxypyridine
- Packaging
- 1g
- Price
- $80
- Updated
- 2021/12/16
- Product number
- 4H07-9-X7
- Product name
- 2-Bromo-5-ethoxypyridine
- Packaging
- 1g
- Price
- $88
- Updated
- 2021/12/16
2-BROMO-5-ETHOXYPYRIDINE Chemical Properties,Usage,Production
Synthesis
55717-45-8
75-03-6
42834-01-5
Sodium hydride (60% dispersed in mineral oil, 0.644 g, 16.09 mmol) was added batchwise to a solution of N,N-dimethylformamide (DMF, 20 mL) of 6-bromopyridin-3-ol (2.0 g, 11.49 mmol) at room temperature and the reaction mixture was stirred for 30 min at 0 °C. Subsequently, iodoethane (1.858 mL, 22.99 mmol) was slowly added dropwise and the reaction mixture was continued to be stirred at room temperature for 3.5 hours. Upon completion of the reaction, the reaction was quenched by adding water to the mixture and the organic phase was extracted with ethyl acetate. The combined organic layers were washed sequentially with water and saturated saline, dried over anhydrous magnesium sulfate and concentrated under reduced pressure to remove the solvent. The crude product was purified by silica gel column chromatography (eluent: hexane-ethyl acetate gradient elution) to afford 2-bromo-5-ethoxypyridine (2.32 g, 100% yield). The product was characterized by 1H-NMR (CDCl3): δ 8.03 (1H, d, J = 2.75 Hz), 7.35 (1H, d, J = 8.69 Hz), 7.07 (1H, dd, J = 8.62, 2.97 Hz), 4.05 (2H, q, J = 6.91 Hz), 1.43 (3H, t, J = 6.94 Hz).
References
[1] Patent: EP2752410, 2014, A1. Location in patent: Paragraph 0441-0443
[2] Patent: WO2012/74126, 2012, A1. Location in patent: Page/Page column 335; 336
2-BROMO-5-ETHOXYPYRIDINE Preparation Products And Raw materials
Raw materials
Preparation Products
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