CAS 76006-09-2

1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one

Description:

1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one is a heterocyclic organic compound characterized by its unique pyrazolo-pyridine structure. This compound features a fused ring system that includes both a pyrazole and a pyridine moiety, contributing to its potential biological activity. It typically appears as a solid at room temperature and may exhibit moderate solubility in polar solvents. The presence of the carbonyl group in the 7-position enhances its reactivity and may facilitate interactions with biological targets. This compound is of interest in medicinal chemistry due to its potential pharmacological properties, including anti-inflammatory and analgesic effects. Its structure allows for various substitutions, which can lead to derivatives with enhanced activity or selectivity. As with many heterocycles, the electronic properties of the nitrogen atoms in the rings can influence its reactivity and interaction with other molecules. Overall, 1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one represents a versatile scaffold for drug development and research in organic synthesis.

Formula: C₆H₅N₃O

InChI: InChI=1S/C6H5N3O/c10-6-5-4(1-2-7-6)3-8-9-5/h1-3H,(H,7,10)(H,8,9)

InChI key: InChIKey=RPXFCERITFUFCN-UHFFFAOYSA-N

SMILES: O=C1C2=C(C=CN1)C=NN2

Synonyms:

• 7H-Pyrazolo[3,4-c]pyridin-7-one, 1,6-dihydro-
• 1H-Pyrazolo[3,4-c]pyridin-7-ol
• 1H,6H,7H-Pyrazolo[3,4-c]pyridin-7-one
• 1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one
• 1,6-Dihydro-pyrazolo[3,4-c]pyridin-7-one

1,6-DIHYDRO-7H-PYRAZOLO[3,4-C]PYRIDIN-7-ONE

CAS: 76006-09-2

Formula: C₆H₅N₃O

Purity: 97%

Color and Shape: Solid

Molecular weight: 135.1234

Ref: IN-DA0058WP

1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one

CAS: 76006-09-2

Purity: 95%

Molecular weight: 135.1260071

Ref: 10-F604541

1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one

CAS: 76006-09-2

1,6-Dihydro-7H-pyrazolo[3,4-c]pyridin-7-one is an isoamyl, pyridine, pyrazole ring that is synthesized from 1,6-dihydro-7H-pyrazolo[3,4-c]pyridin-7-one. This compound has the ability to catalyze the deacetylation of acetyl compounds in a process that involves potassium carbonate and copper. The reaction between 1,6-dihydro-7H-pyrazolo[3,4-c]pyridin-7-one and nitrite yields acetyl radicals. The acetyl radicals then react with methoxyl groups to form ethoxy radicals. Ethoxy radicals are more reactive than acetyl radicals and can be used to produce other organic or inorganic compounds.

Formula: C₆H₅N₃O

Purity: Min. 95%

Molecular weight: 135.12 g/mol

Ref: 3D-BDA00609