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5-AMINO-2-NITROPYRIDINE

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Products Intro: CAS:14916-65-5
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG
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Products Intro: Product Name:6-Nitropyridin-3-amine
CAS:14916-65-5
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CAS:14916-65-5
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Products Intro: Product Name:5-AMINO-2-NITROPYRIDINE
CAS:14916-65-5
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Products Intro: Product Name:5-AMINO-2-NITROPYRIDINE
CAS:14916-65-5
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5-AMINO-2-NITROPYRIDINE manufacturers

  • 5-AMINO-2-NITROPYRIDINE
  • 5-AMINO-2-NITROPYRIDINE pictures
  • $1.10 / 1g
  • 2025-11-18
  • CAS:14916-65-5
  • Min. Order: 1g
  • Purity: 99.00%
  • Supply Ability: 100 Tons min
5-AMINO-2-NITROPYRIDINE Basic information
Product Name:5-AMINO-2-NITROPYRIDINE
Synonyms:5-AMINO-2-NITROPYRIDINE;3-Amino-6-nitropyridine;3-Pyridinamine,6-nitro-(9CI);6-Nitropyridin-3-amine;2-Nitro-5-pyridinamine;6-Nitro-pyridin-3-ylamine;5-Amino-2-nitropyridine 95%;6-nitro-3-PyridinaMine
CAS:14916-65-5
MF:C5H5N3O2
MW:139.11
EINECS:
Product Categories:Pyridines;Building Blocks;Pyridine;Heterocycle-Pyridine series;NITRO
Mol File:14916-65-5.mol
5-AMINO-2-NITROPYRIDINE Structure
5-AMINO-2-NITROPYRIDINE Chemical Properties
Melting point 234-235 °C (decomp)(Solv: benzene (71-43-2))
Boiling point 382.9±22.0 °C(Predicted)
density 1.437±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka-1.02±0.10(Predicted)
AppearanceYellow to brown Solid
Safety Information
HS Code 2933599590
MSDS Information
5-AMINO-2-NITROPYRIDINE Usage And Synthesis
Uses6-Nitropyridin-3-amine is used in preparation of dihydroquinazoline compounds as NAV1.8 inhibitors.
Synthesis
5-Chloro-2-nitropyridine

52092-47-4

5-AMINO-2-NITROPYRIDINE

14916-65-5

General procedure for the synthesis of 5-amino-2-nitropyridine from 2-nitro-5-chloropyridine: To a solution of 5-chloro-2-nitropyridine (3 g, 19 mmol) in ethanol (EtOH, 30 mL) was added saturated ammonia (NH3-H2O, 20 mL). The reaction mixture was placed in an autoclave and the reaction was stirred at 50 psi pressure and 150 °C overnight. The progress of the reaction was monitored by thin layer chromatography (TLC) and after confirming the completion of the reaction, the reaction mixture was cooled to room temperature. The resulting solid product was collected by filtration and washed with petroleum ether (PE, 100 mL) to afford 5-amino-2-nitropyridine (0.7 g, yield: 26%) as a yellow solid. Mass spectrometry (MS) analysis showed: m/z 140.1 ([M+H]+).

References[1] Patent: WO2013/126608, 2013, A1. Location in patent: Paragraph 00647
5-AMINO-2-NITROPYRIDINE Preparation Products And Raw materials
Raw materials5-Chloro-2-nitropyridine-->Water-->Ethanol-->Ammonia
Tag:5-AMINO-2-NITROPYRIDINE(14916-65-5) Related Product Information
2,5-DINITROPYRIDINE 5-AMINO-2-NITROPYRIDINE 6-Nitro-2,5-diaminopyridine 4-(ETHYLAMINO)-3-NITROPYRIDINE 2-Amino-6-[(4-fluorobenzyl)-amino]-3-nitropyridine 5-Amino-3-nitropyridine,3-AMINO-5-NITROPYRIDINE,3-AMINO-5-NITROPYRIDINE 97%,3-Amino-5-nitropyridine97% METHYL 4-AMINO-5-NITROPYRIDINE-2-CARBOXYLATE 2-Amino-6-methyl-5-nitropyridine 3-AMINO-2-NITROPYRIDINE 2-METHYLAMINO-5-NITROPYRIDINE 2-Amino-6-nitropyridine97%,2-AMINO-6-NITROPYRIDINE 97%,2-AMINO-6-NITROPYRIDINE 2-Acetamido-5-nitropyridine 4-BENZYLAMINO-3-NITROPYRIDINE 2-AMINO-4-NITROPYRIDINE-N-OXIDE 4-AMINO-2-NITROPYRIDINE,4-Amino-2-nitropyridine97%,4-AMINO-2-NITROPYRIDINE 97% 4-ACETAMIDO-3-NITROPYRIDINE 2-Amino-3-methyl-5-nitropyridine 4-Amino-3-nitropyridine ,98%,4-AMINO-3-NITROPYRIDINE

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