CAS 101083-92-5

5-nitro-1H-Pyrrolo[2,3-B]pyridine

Description:

5-Nitro-1H-pyrrolo[2,3-b]pyridine is a heterocyclic organic compound characterized by its fused pyrrole and pyridine rings, which contribute to its unique chemical properties. The presence of a nitro group at the 5-position enhances its reactivity and polar character, making it a potential candidate for various chemical reactions, including electrophilic substitutions. This compound typically exhibits a pale yellow to brownish color and is soluble in polar organic solvents. Its molecular structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, the compound may exhibit interesting electronic properties owing to the conjugation between the nitrogen atoms and the aromatic system. Safety data should be consulted, as nitro compounds can be hazardous and may require careful handling. Overall, 5-nitro-1H-pyrrolo[2,3-b]pyridine is a valuable compound in research and development within the fields of organic and medicinal chemistry.

Formula: C₇H₅N₃O₂

InChI: InChI=1/C7H5N3O2/c11-10(12)6-3-5-1-2-8-7(5)9-4-6/h1-4H,(H,8,9)

SMILES: c1cnc2c1cc(c[nH]2)N(=O)=O

Synonyms:

• 5-Nitro-7-Azaindole
• 1H-Pyrrolo[2,3-b]pyridine, 5-nitro-

1H-Pyrrolo[2,3-b]pyridine, 5-nitro-

CAS: 101083-92-5

Formula: C₇H₅N₃O₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 163.1335

Ref: IN-DA0003PJ

5-Nitro-1H-pyrrolo[2,3-b]pyridine

CAS: 101083-92-5

5-Nitro-1H-pyrrolo[2,3-b]pyridine

Formula: C₇H₅N₃O₂

Purity: 97%

Color and Shape: yellow solid

Molecular weight: 163.13g/mol

Ref: 54-OR308037

5-Nitro-7-azaindole

CAS: 101083-92-5

Formula: C₇H₅N₃O₂

Purity: 95%

Color and Shape: Solid

Molecular weight: 163.136

Ref: 10-F080031

5-Nitro-7-azaindole

CAS: 101083-92-5

5-Nitro-7-azaindole is a heterocyclic compound that is structurally related to the furoquinolines. It has been shown to act as an inhibitor of benzene and pyridine oxidases, which are enzymes that catalyze the conversion of these compounds into reactive intermediates. The reaction mechanism of 5-Nitro-7-azaindole with benzene and pyridine oxidases involves the formation of covalent bonds with reactive sulfur atoms in the enzyme active site. 5-Nitro-7-azaindole also inhibits bacterial growth by inhibiting DNA synthesis. This compound has been found to be scalable and can be produced at large scales without loss in quality. 5-Nitro-7-azaindole is not stereoselective and it is not an aromatic system, meaning that it does not have a benzene ring.

Formula: C₇H₅N₃O₂

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 163.13 g/mol

Ref: 3D-FN15227

5-Nitro-1H-pyrrolo[2,3-b]pyridine

Controlled Product

CAS: 101083-92-5

Formula: C₇H₅N₃O₂

Color and Shape: Neat

Molecular weight: 163.133

Ref: TR-N520120