CAS 3346-63-2

3-Nitro-2,6-pyridinediamine

Description:

3-Nitro-2,6-pyridinediamine, with the CAS number 3346-63-2, is an organic compound that features a pyridine ring substituted with amino and nitro groups. This compound is characterized by its aromatic nature due to the presence of the pyridine ring, which contributes to its stability and reactivity. The nitro group (-NO2) is a strong electron-withdrawing group, which can influence the compound's reactivity in various chemical reactions, particularly in electrophilic substitution. The amino groups (-NH2) provide basic properties and can participate in hydrogen bonding, making the compound potentially useful in various applications, including pharmaceuticals and agrochemicals. Additionally, the presence of multiple functional groups allows for diverse chemical transformations, enhancing its utility in synthetic organic chemistry. Safety data should be consulted, as nitro compounds can be sensitive and may pose health risks. Overall, 3-Nitro-2,6-pyridinediamine is a versatile compound with significant implications in chemical research and industry.

Formula: C₅H₆N₄O₂

InChI: InChI=1S/C5H6N4O2/c6-4-2-1-3(9(10)11)5(7)8-4/h1-2H,(H4,6,7,8)

InChI key: InChIKey=TZEVSKPZTQIPLS-UHFFFAOYSA-N

SMILES: N(=O)(=O)C1=C(N)N=C(N)C=C1

Synonyms:

• 2,6-Diamino-3-fluoropyridine
• 2,6-Diamino-3-nitropyridine
• 2,6-Pyridinediamine, 3-nitro-
• 3-Nitro-2,6-pyridinediamine
• NSC 404692
• Pyridine, 2,6-diamino-3-nitro-

TERT-BUTYL CARBAZATE

CAS: 3346-63-2

Formula: C₅H₆N₄O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 154.1267

Ref: IN-DA00C6UB

3-Nitropyridine-2,6-diamine

CAS: 3346-63-2

3-Nitropyridine-2,6-diamine

Purity: 97%

Molecular weight: 154.13g/mol

Ref: 54-OR79931

3-Nitropyridine-2,6-diamine

CAS: 3346-63-2

Formula: C₅H₆N₄O₂

Purity: 97%

Color and Shape: Solid

Molecular weight: 154.129

Ref: 10-F464212

2,6-diamino-3-nitropyridine

CAS: 3346-63-2

2,6-Diamino-3-nitropyridine is a chemical compound that has been used as a catalyst for hydrogenation reduction in the synthesis of various organic compounds. It is a colorless solid that can be obtained by reacting ethyl chloroformate with ammonia and pyridine. 2,6-Diamino-3-nitropyridine can also be synthesized by ammonolysis of chloroformates or maleates with ammonia. The reaction mechanism of this process is similar to that of the catalytic hydrogenation reduction. This chemical is used in the preparation of flupirtine maleate, an anti-inflammatory drug with analgesic properties.

Formula: C₅H₆N₄O₂

Purity: Min. 95%

Molecular weight: 154.13 g/mol

Ref: 3D-DAA34663