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Home > Encyclopedia > 3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE structure

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE 

structure
  • CAS No:

    102830-75-1

  • Formula:

    C6H5BrClNO

  • Chemical Name:

    3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE

  • Synonyms:

    3-Bromo-5-chloro-2-methoxypyridine;2-Methoxy-3-Bromo-5-Chloropyridine;3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE;PYRIDINE, 3-BROMO-5-CHLORO-2-METHOXY-;MFCD08059322;PubChem6584;SCHEMBL3634770;CTK4A1525;DTXSID70544002;ABBYPHARMA AP-11-5380

  • Categories:

    Pharmaceutical Intermediates  >  Bulk Drug Intermediates

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Basic Attributes

222.47

220.924301

DTXSID70544002

2933399090

Characteristics

22.1

2.5

1.650±0.06 g/cm3(Predicted)

49.0 to 53.0 °C

215.8±35.0 °C(Predicted)

84.3±25.9 °C

1.560

0.212mmHg at 25°C

Safety Information

IRRITANT

UN 2811 6.1 / PGIII

25

45

T

P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501

H315

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 4 companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

3-BROMO-5-CHLORO-2-METHOXY-PYRIDINE Use and Manufacturing

PREPARATION 13; (5-Chloro-2-methoxypyridin-3-yl)boronic acid a) 3-Bromo-5-chloro-2-methoxypyridineA solution of bromine (1.5 mL, 29.28 mmol) in glacial acetic acid (7 mL) was slowly added to a mixture of 5-chloro-2-methoxypyridine (2.1 g, 14.63 mmol) and sodium acetate (1.2 g, 14.63 mmol) in glacial acetic acid (7 mL) and the resulting mixture was stirred at 80 °C for 6 hours. The reaction was allowed to cool down to ambient temperature and then diethyl ether and water were added. The organic layer was separated, washed with a 1N aqueous solution of sodium hydroxide and a 4percent aqueous solution of sodium bisulphite, dried over magnesium sulphate and the solvent removed under reduced pressure. The residue was purified by flash chromatography (100percent hexanes) to give the title compound (2.1 g, 64percent) as a white solid.PREPARATION 13; (5-Chloro-2-methoxypyridin-3-yl)boronic acid a) 3-Bromo-5-chloro-2-methoxypyridine A solution of bromine (1.5 mL, 29.28 mmol) in glacial acetic acid (7 mL) was slowly added to a mixture of 5-chloro-2-methoxypyridine (2.1 g, 14.63 mmol) and sodium acetate (1.2 g, 14.63 mmol) in glacial acetic acid (7 mL) and the resulting mixture was stirred at 80 C for 6 hours. The reaction was allowed to cool down to room temperature and then diethyl ether and water were added. The organic layer was separated, washed with a 1 N aqueous solution of sodium hydroxide and a 4percent aqueous solution of sodium bisulphite, dried over magnesium sulphate and the solvent removed under reduced pressure. The residue was purified by flash chromatography (100percent hexanes) to give the title compound (2.1 g, 64percent) as a white solid. To a mixture of To a mixture of To a stirred solution of

Computed Properties

Molecular Weight:222.47
XLogP3:2.5
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:220.92430
Monoisotopic Mass:220.92430
Topological Polar Surface Area:22.1
Heavy Atom Count:10
Complexity:114
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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