Production Method 1

914942-85-1

887147-20-8

Reaction Conditions

1.1 Reagents: Sulfuric acid Solvents: Water ;  12 h, rt

Reference

Synthesis and evaluation of novel imidazo[4,5-c]pyridine derivatives as antimycobacterial agents against Mycobacterium tuberculosis

Madaiah, Malavalli; Prashanth, Maralekere K.; Revanasiddappa, Hosakere D.; Veeresh, Bantal, New Journal of Chemistry, 2016, 40(11), 9194-9204

2,6-dichloro-N-methyl-3-nitro-pyridin-4-amine Raw materials

• 4-Pyridinamine, 2,6-dichloro-N-methyl-N-nitro-

2,6-dichloro-N-methyl-3-nitro-pyridin-4-amine Preparation Products

• 2,6-dichloro-N-methyl-3-nitro-pyridin-4-amine (887147-20-8)

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• 2. Evolution study of photo-synthesized gold nanoparticles by spectral deconvolution model: a quantitative approach
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• 4. Evolution in surface coverage of CH3NH3PbI3?XClXvia heat assisted solvent vapour treatment and their effects on photovoltaic performance of devices
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• 5. Evolved polymerases facilitate selection of fully 2′-OMe-modified aptamers?
  Zhixia Liu,Tingjian Chen,Floyd E. Romesberg Chem. Sci., 2017,8, 8179-8182

• 2604-39-9(2-chloro-5-nitro-pyridin-4-amine)
• 2789-25-5(2-chloro-3-nitropyridin-4-amine)
• 89276-22-2(1,5-Naphthyridin-4-amine, 2-chloro-3-nitro-)
• 16013-85-7(2,6-dichloro-3-nitro-pyridine)
• 2897-43-0(2,6-dichloro-3-nitro-pyridin-4-amine)
• 405230-91-3(2,5-Dichloro-3-nitropyridin-4-amine)
• 182257-03-0(2-Chloro-N,6-dimethyl-3-nitropyridin-4-amine)
• 87992-37-8(1,6-Naphthyridin-4-amine, 2-chloro-3-nitro-)
• 1092352-67-4(3-Amino-2-chloro-4-nitropyridine)
• 607373-89-7(4-Pyridinamine, 2-chloro-N-ethyl-5-nitro-)