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22918-01-0

22918-01-0 Structure

22918-01-0 Structure
IdentificationMore
[Name]

2-Bromo-4-chloropyridine
[CAS]

22918-01-0
[Synonyms]

2-BROMO-4-CHLOROPYRIDINE
4-CHLORO-2-BROMOPYRIDINE
[Molecular Formula]

C5H3BrClN
[MDL Number]

MFCD03840757
[Molecular Weight]

192.44
[MOL File]

22918-01-0.mol
Chemical PropertiesBack Directory
[Appearance]

Light yellow liquid
[Melting point ]

<30℃
[Boiling point ]

98°C
[density ]

1.736±0.06 g/cm3(Predicted)
[Fp ]

>110℃
[storage temp. ]

-20°C
[solubility ]

soluble in Methanol
[form ]

powder to lump to clear liquid
[pka]

0.12±0.10(Predicted)
[color ]

White or Colorless to Almost white or Almost colorless
[InChI]

InChI=1S/C5H3BrClN/c6-5-3-4(7)1-2-8-5/h1-3H
[InChIKey]

SURKZMFXICWLHU-UHFFFAOYSA-N
[SMILES]

C1(Br)=NC=CC(Cl)=C1
[CAS DataBase Reference]

22918-01-0(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)Exclamation Mark (GHS07)
GHS05,GHS07
[Signal word ]

Danger
[Hazard statements ]

H302-H315-H318-H335
[Precautionary statements ]

P280-P301+P312+P330-P302+P352-P305+P351+P338+P310
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[WGK Germany ]

1
[HS Code ]

2933399990
[Storage Class]

10 - Combustible liquids
[Hazard Classifications]

Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Chemical Properties]

Light yellow liquid
[Uses]

2-Bromo-4-chloropyridine is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
[Synthesis]

To an aqueous solution of 48 % strength hydrobromic acid (82 rnL) at 0 0C was added 4-chloro-2-pyridinamine (8.9 g, 69.2 mmol) followed by addition of bromine (33.4 g, 209 mmol) over 10 min. The resulting mixture was cooled to -10 0C, and a solution of NaNO2 (10.65 g, 154 mmol) in H2O (20 rnL) was poured over 30 min. The mixture was warmed at room temperature and stirred overnight. The mixture was cooled to 0 0C, and NaOH (35 %) was added until the pH >10. The mixture was then extracted with ethyl acetate. The organic layer was then dried, filtered, and concentrated in vacuo. The product was purified via column chromatography (0-20 per cent ethyl acetate/hexane) to afford 2-bromo-4-chloropyridine (12.1 g, 92 %).
[References]

[1] Patent: WO2008/124575, 2008, A1. Location in patent: Page/Page column 110; 111
[2] Patent: WO2008/124582, 2008, A1. Location in patent: Page/Page column 92-93
[3] Patent: WO2003/99274, 2003, A1. Location in patent: Page 562-563
Spectrum DetailBack Directory
[Spectrum Detail]

2-Bromo-4-chloropyridine(22918-01-0)1HNMR
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