CAS 104675-26-5

9-amino-3,4-dihydroacridin-1(2H)-one

Description:

9-Amino-3,4-dihydroacridin-1(2H)-one is an organic compound characterized by its acridine backbone, which is a fused ring system known for its aromatic properties. This compound features an amino group (-NH2) and a carbonyl group (C=O) within its structure, contributing to its reactivity and potential biological activity. The presence of the dihydro form indicates that it has two hydrogen atoms added to the aromatic system, which can influence its electronic properties and stability. It is typically a solid at room temperature and may exhibit solubility in polar solvents due to the presence of the amino group. This compound is of interest in medicinal chemistry, particularly for its potential applications in pharmaceuticals, as acridine derivatives are known for their diverse biological activities, including antimicrobial and antitumor properties. Additionally, its unique structure may allow for further modifications to enhance its efficacy or selectivity in various chemical reactions or biological interactions.

Formula: C₁₃H₁₂N₂O

InChI: InChI=1/C13H12N2O/c14-13-8-4-1-2-5-9(8)15-10-6-3-7-11(16)12(10)13/h1-2,4-5H,3,6-7H2,(H2,14,15)

InChI key: InChIKey=JUSJJSHTMCPMOX-UHFFFAOYSA-N

SMILES: NC1=C2C(=NC=3C1=CC=CC3)CCCC2=O

Synonyms:

• 1(2H)-Acridinone, 9-amino-3,4-dihydro-
• 9-Amino-3,4-dihydro-1(2H)-acridinone
• 9-Amino-3,4-dihydroacridin-1(2H)-one
• 9-Amino-3,4-dihydroacridin-1(2H)-one
• 9-AMino-3,4-dihydro-2H-acridin-1-one

9-Amino-3,4-dihydroacridin-1(2H)-one

Controlled Product

CAS: 104675-26-5

Applications Intermediate in the preparation of Mentane.
References Shutske, G., et al.: Bioorg. Med. Chem. Lett., 2, 865 (1992),

Formula: C₁₃H₁₂N₂O

Color and Shape: Neat

Molecular weight: 212.25

Ref: TR-A604880