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3-Bromo-4-chloropyridine

3-Bromo-4-chloropyridine Suppliers list
Company Name: Fuxin Yuke Chemical Technology Co., Ltd.  Gold
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Company Name: J & K SCIENTIFIC LTD.  
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Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
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3-Bromo-4-chloropyridine manufacturers

3-Bromo-4-chloropyridine Basic information
Product Name:3-Bromo-4-chloropyridine
Synonyms:3-BROMO-4-CHLOROPYRIDINE;4-CHLORO-3-BROMOPYRIDINE;3-BroMo-4-chloropyridine, 98% 1GR;3-BroMo-4-chloridepyridine;3-Bromo-4-chloropyridine,98%;3-BroMo-2-chloropyridine, 97+%;3-broMo -4-chlorine pyridine;Pyridine, 3-bromo-4-chloro-
CAS:36953-42-1
MF:C5H3BrClN
MW:192.44
EINECS:690-646-5
Product Categories:Pyridine;Pyridine series;Halides;Pyridines
Mol File:36953-42-1.mol
3-Bromo-4-chloropyridine Structure
3-Bromo-4-chloropyridine Chemical Properties
Melting point 17.5-18.5 °C
Boiling point 115 °C(Press: 20 Torr)
density 1.19
refractive index 1.453
storage temp. Inert atmosphere,Store in freezer, under -20°C
form Liquid After Melting
pka1.74±0.10(Predicted)
color Clear colorless to yellow
InChIInChI=1S/C5H3BrClN/c6-4-3-8-2-1-5(4)7/h1-3H
InChIKeyQADXKWUCCGPQNR-UHFFFAOYSA-N
SMILESC1=NC=CC(Cl)=C1Br
CAS DataBase Reference36953-42-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi,T
Risk Statements 36/37/38-20/22-41-37/38-25
Safety Statements 36/37/39-26-22-45-39
WGK Germany WGK 3
HazardClass IRRITANT
HS Code 29333990
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
ACROS English
3-Bromo-4-chloropyridine Usage And Synthesis
Chemical PropertiesLight yellow needles
Uses 3-Bromo-4-chloropyridine can be used as a bulk drug intermediate in pharmaceutical synthesis.
Synthesis
4-CHLOROFURO[3,2-C]PYRIDINE

31270-80-1

3-Bromo-4-chloropyridine

36953-42-1

3-Bromo-4-chlorofuro[3,2-c]pyridine

220939-72-0

Example 543A Synthesis of 3-bromo-4-chlorofuro[3,2-c]pyridine: 4-Chlorofuro[3,2-c]pyridine (commercially available, 10.60 g, 69 mmol) was dissolved in carbon tetrachloride (135 mL) and cooled to -15°C. Bromine (12.13 g, 80 mmol) was added dropwise over 15 min. The reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, the solvent was removed under vacuum. The residue was dissolved in methanol (250 mL), 20% aqueous sodium hydroxide solution (35 mL) was added and stirring was continued for 1 hour at room temperature. Subsequently, methanol was removed under vacuum and the residue was partitioned between water (100 mL) and dichloromethane (50 mL). The organic layers were combined, dried over anhydrous magnesium sulfate, and the solvent was removed in vacuo to afford 3-bromo-4-chlorofuro[3,2-c]pyridine 15.45 g (96% yield) as a solid. Mass spectrum (ESI(+)) m/e 232,234 (M + H)+.

References[1] Patent: US2005/26944, 2005, A1
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