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4-Amino-3-bromopyridine

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Products Intro: Product Name:4-Amino-3-bromopyridine
CAS:13534-98-0
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Products Intro: Product Name:3-Bromo-4-pyridinamine
CAS:13534-98-0
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4-Amino-3-bromopyridine manufacturers

  • 3-Bromo-4-pyridinamine
  • 3-Bromo-4-pyridinamine pictures
  • $200.00 / 1KG
  • 2025-09-25
  • CAS:13534-98-0
  • Min. Order: 1KG
  • Purity: 99%, 99.5% Sublimated
  • Supply Ability: g-kg-tons, free sample is available
  • 4-Amino-3-bromopyridine
  • 4-Amino-3-bromopyridine pictures
  • $0.00 / 25KG
  • 2025-08-13
  • CAS:13534-98-0
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: 50000KG/month
4-Amino-3-bromopyridine Basic information
Product Name:4-Amino-3-bromopyridine
Synonyms:IFLAB-BB F3250-0675;AKOS BBS-00005959;AKOS PAO-0460;1H-PYRAZOLE-5-CARBOXYLIC ACID;4-AMINO-3-BROMOPYRIDINE;3-Bromo-4-aminopyridine;3-Bromo-4-pyridinamine;3-Bromo-4-aminopyridine, 3-Bromo-4-pyridinamine
CAS:13534-98-0
MF:C5H5BrN2
MW:173.01
EINECS:628-420-5
Product Categories:Amines;Pyridines;Pyridine
Mol File:13534-98-0.mol
4-Amino-3-bromopyridine Structure
4-Amino-3-bromopyridine Chemical Properties
Melting point 61-69 °C
Boiling point 275.8±20.0 °C(Predicted)
density 1.6065 (rough estimate)
refractive index 1.5182 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pkapK1: 7.04(+1) (20°C)
form Crystalline Powder
color White to off-white
BRN 110183
InChIInChI=1S/C5H5BrN2/c6-4-3-8-2-1-5(4)7/h1-3H,(H2,7,8)
InChIKeyDDQYSZWFFXOXER-UHFFFAOYSA-N
SMILESC1=NC=CC(N)=C1Br
CAS DataBase Reference13534-98-0(CAS DataBase Reference)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 36/37/38-41-37/38-22
Safety Statements 26-36/37/39-37/39-39
WGK Germany 3
HazardClass IRRITANT, AIR SENSITIVE
HS Code 29333990
MSDS Information
ProviderLanguage
3-Bromo-4-aminopyridine English
4-Amino-3-bromopyridine Usage And Synthesis
Chemical Propertiesyellow Cryst
Synthesis
4-Aminopyridine

504-24-5

4-Amino-3-bromopyridine

13534-98-0

General procedure for the synthesis of 4-amino-3-bromopyridine from 4-aminopyridine: To a mixture of 4-aminopyridine (20.0 g, 0.21 mol) and acetonitrile (300.0 mL) was added N-bromosuccinimide (NBS) (39.8 g, 0.22 mol) in batches at 0 °C, the reaction was to be carried out protected from light. Subsequently, the reaction mixture was stirred at room temperature for 24 hours. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the mixture was cooled to room temperature and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by fast column chromatography (silica gel as stationary phase and dichloromethane/methanol=20:1 as eluent) to afford the target compound 4-amino-3-bromopyridine (33.2 g, 91.4% yield) as a light yellow solid. Mass spectrum (ESI) m/z: 172.9 [M + H]+.

References[1] European Journal of Medicinal Chemistry, 2016, vol. 120, p. 37 - 50
[2] Organic and Biomolecular Chemistry, 2017, vol. 15, # 15, p. 3216 - 3231
[3] Patent: US2003/22883, 2003, A1
[4] Journal of the American Chemical Society, 2012, vol. 134, # 31, p. 12928 - 12931
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