ChemicalBook > CAS DataBase List > 2-BROMO-5-ETHOXYPYRIDINE

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
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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
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Safety

HS Code 
2933399990
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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.

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N-Bromosuccinimide Price

TRC
Product number
B696068
Product name
2-Bromo-5-ethoxypyridine
Packaging
1g
Price
$165
Updated
2021/12/16
AK Scientific
Product number
V5913
Product name
2-Bromo-5-ethoxypyridine
Packaging
5g
Price
$263
Updated
2021/12/16
Apolloscientific
Product number
OR3575
Product name
2-Bromo-5-ethoxypyridine
Packaging
5g
Price
$319
Updated
2021/12/16
Apolloscientific
Product number
OR3575
Product name
2-Bromo-5-ethoxypyridine
Packaging
1g
Price
$80
Updated
2021/12/16
SynQuest Laboratories
Product number
4H07-9-X7
Product name
2-Bromo-5-ethoxypyridine
Packaging
1g
Price
$88
Updated
2021/12/16
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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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2-BROMO-5-ETHOXYPYRIDINE Suppliers

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