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2-Bromo-5-nitropyridine

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2-Bromo-5-nitropyridine Basic information

Product Name:
2-Bromo-5-nitropyridine
Synonyms:
  • TIMTEC-BB SBB003519
  • 2-BROMO-5-NITROPYRIDINE
  • 2-BROMO-5-NITROPYRIDINE 97%
  • 2-BROMO-5-NITROPYRIDINE 2-BROMO-5-NITROPYRIDINE
  • 2-BORMO-5-NITROPYRIDINE
  • 2-BroMo-5-nitropyridine, 98% 1GR
  • 5-Nitro-2-broMopyridine
  • NSC 73702
CAS:
4487-59-6
MF:
C5H3BrN2O2
MW:
202.99
EINECS:
224-777-2
Product Categories:
  • Brominated heterocyclic series
  • Boronic Acid
  • Pyridines derivates
  • C5Heterocyclic Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyridine series
  • Halides
  • Pyridine
  • Nucleotides and Nucleosides
  • Bromopyridines
  • Halopyridines
  • Bases & Related Reagents
  • Nucleotides
  • compounds of pyridine
  • pyridines
  • blocks
  • Bromides
  • NitroCompounds
  • pyridine derivative
  • Pyridines, Pyrimidines, Purines and Pteredines
  • Building Blocks/Intermediates
Mol File:
4487-59-6.mol
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2-Bromo-5-nitropyridine Chemical Properties

Melting point:
139-141 °C (lit.)
Boiling point:
145-147 °C/10 mmHg (lit.)
Density 
1.8727 (rough estimate)
refractive index 
1.6200 (estimate)
Flash point:
145-147°C/10mm
storage temp. 
Inert atmosphere,2-8°C
solubility 
Chloroform, Hot Methanol
form 
Crystalline Powder
pka
-3.24±0.10(Predicted)
color 
Light yellow to light brown
Water Solubility 
Insoluble in water.
BRN 
120901
InChIKey
HUUFTVUBFFESEN-UHFFFAOYSA-N
CAS DataBase Reference
4487-59-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-36/37/38-20/21/22
Safety Statements 
26-37/39-22-36
RIDADR 
UN 2811 6.1/PG 3
WGK Germany 
3
Hazard Note 
Irritant/Keep Cold
HazardClass 
IRRITANT, IRRITANT-HARMFUL
PackingGroup 
III
HS Code 
29333990

MSDS

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2-Bromo-5-nitropyridine Usage And Synthesis

Chemical Properties

Off-white to light yellow crystal.

Uses

2-Bromo-5-nitropyridine was used in preparation of boc-protected (piperazin-1-ylmethyl)biaryls via microwave-mediated Suzuki-Miyaura coupling with (boc-piperazin-1-ylmethyl)phenylboronic acid pinacol esters. It was also used in the synthesis of 2-pyridyl analogs. Substituted 5-nitro-2-ethynylpyridines were synthesized by the Sonogashira reaction of 2-bromo-5-5-nitropyridine with terminal acetylenes.

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