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4-Amino-2-bromopyridine

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4-Amino-2-bromopyridine Basic information

Product Name:
4-Amino-2-bromopyridine
Synonyms:
  • 4-Amino-2-bromopyridine 95%
  • 2-bromo-4-pyridinamin
  • IFLAB-BB F1371-0175
  • AKOS BBS-00001327
  • 2-BROMOPYRIDIN-4-AMINE
  • 2-BROMO-PYRIDIN-4-YLAMINE
  • 2-BROMO-4-PYRIDINAMINE
  • 2-BROMO-4-PYRIDYLAMINE
CAS:
7598-35-8
MF:
C5H5BrN2
MW:
173.01
EINECS:
629-178-3
Product Categories:
  • Pyridine series
  • Amines
  • Pyridines
  • Pyridines derivates
  • Pyridine
  • Pyridines, Pyrimidines, Purines and Pteredines
Mol File:
7598-35-8.mol
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4-Amino-2-bromopyridine Chemical Properties

Melting point:
92-96 °C
Boiling point:
321.3±22.0 °C(Predicted)
Density 
1.710±0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
4.89±0.30(Predicted)
form 
Crystalline Powder or Powder
color 
White to pale brown to orange
Water Solubility 
Slightly soluble in water.
BRN 
108928
InChI
InChI=1S/C5H5BrN2/c6-5-3-4(7)1-2-8-5/h1-3H,(H2,7,8)
InChIKey
GNTGEMWEXKBWBX-UHFFFAOYSA-N
SMILES
C1(Br)=NC=CC(N)=C1
CAS DataBase Reference
7598-35-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
22-37/38-41-36/37/38-20/21/22
Safety Statements 
26-36/37/39-36/37/38-36-36/37
WGK Germany 
3
Hazard Note 
Harmful/Irritant
HazardClass 
IRRITANT
HS Code 
29333990
Storage Class
11 - Combustible Solids
Hazard Classifications
Acute Tox. 4 Oral
Eye Dam. 1
Skin Irrit. 2
STOT SE 3

MSDS

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4-Amino-2-bromopyridine Usage And Synthesis

Chemical Properties

Light yellow Cryst

Uses

4-Amino-2-bromopyridine is used as medical intermediate.

Synthesis

A conventional synthetic route toward 4-amino-2-bromopyridine starts from its precursor, 2-bromo-4-nitropyridine, where the nitro group is reduced to an amino group via the action of elemental metals. Common reduction systems include iron powder with acetic acid, magnesium powder with titanium tetrachloride, and so forth. Generally, the reduction system using iron powder and acetic acid requires high-temperature conditions for proceeding. After the reaction completes, pyridine tends to form a salt with protic acids, thus pH adjustment is necessary during the post-treatment process to liberate 4-Amino-2-bromopyridine from its salt form.

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