CAS 4214-75-9
:2-Amino-3-nitropyridine
Description:
2-Amino-3-nitropyridine is an organic compound characterized by its pyridine ring, which is a six-membered aromatic heterocycle containing one nitrogen atom. The compound features an amino group (-NH2) and a nitro group (-NO2) positioned at the 2 and 3 positions of the pyridine ring, respectively. This substitution pattern contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. 2-Amino-3-nitropyridine is typically a yellow to orange crystalline solid, and it is soluble in polar solvents like water and alcohols. The presence of both amino and nitro groups makes it a versatile intermediate in organic synthesis, allowing for further functionalization. Additionally, the compound exhibits properties such as being a weak base due to the amino group and can participate in electrophilic aromatic substitution reactions. Safety data indicates that it should be handled with care, as it may pose health risks upon exposure. Overall, 2-Amino-3-nitropyridine is a significant compound in synthetic organic chemistry.
Formula:C5H5N3O2
InChI:InChI=1S/C5H5N3O2/c6-5-4(8(9)10)2-1-3-7-5/h1-3H,(H2,6,7)
InChI key:InChIKey=BPYHGTCRXDWOIQ-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(N)N=CC=C1
Synonyms:- 2-Amino-3-Nitropyridinium
- 2-Pyridinamine, 3-nitro-
- 3-Nitro-2-aminopyridine
- 3-Nitro-2-pyridinamine
- 3-Nitropyridin-2-Amine
- 3-Nitropyridin-2-Ylamine
- NSC 12460
- Pyridine, 2-amino-3-nitro-
- 2-Amino-3-nitropyridine
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
2-Amino-3-nitropyridine
CAS:Formula:C5H5N3O2Purity:>98.0%(T)Color and Shape:Light yellow to Yellow to Orange powder to crystalMolecular weight:139.112-Amino-3-nitropyridine
CAS:<p>2-Amino-3-nitropyridine</p>Formula:C5H5N3O2Purity:98%Color and Shape: yellow solidMolecular weight:139.11g/mol2-Amino-3-nitropyridine
CAS:<p>2-Amino-3-nitropyridine is a synthetic molecule that has the chemical formula C6H7N5O2. It can exist in four different forms, three of which are isomers. These three isomers have different properties, such as melting point and solubility. The synthesis of 2-amino-3-nitropyridine can be achieved through a solid phase synthesis using sodium periodate as the acid catalyst. The reaction mechanism involves nitration of 2-amino pyridine with hydrogen peroxide to produce 3-nitro pyridine followed by hydrolysis to form 2-amino-3 nitropyridine. This reaction produces two dihedral angles in the molecule, one between the nitrogen and oxygen atoms and another between the nitrogen atom and carbon atom bonded to it. The functional groups present on this molecule are an amino group, a nitro group, and an amide group.</p>Purity:Min. 98 Area-%Color and Shape:Yellow SolidMolecular weight:139.11 g/mol





